Basic Information

CYP2C19

Full name: cytochrome P450 family 2 subfamily C member 19

Gene type: protein coding

HGNC ID: HGNC:2621

Gene location: 10q23.33

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/1557

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:2621

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000769.4

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P33261

AlphaFold: https://alphafold.ebi.ac.uk/entry/P33261

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/124020

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=1557

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa00590+1557

Variant resources

Gene	Disease type	Variant type	NCBI dbSNP	Alleles	Variant location
CYP2C19	AMD	Synonymous Variant	rs4244285	G>A / G>C / G>T	chr10:94781859 (GRCh38.p13)