Canonical Allele Identifier: CA5616482
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs750557758

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780554C>G , CM000672.2:g.94780554C>G GRCh38
NC_000010.10:g.96540311C>G , CM000672.1:g.96540311C>G GRCh37
NC_000010.9:g.96530301C>G NCBI36
NG_008384.2:g.22849C>G
NG_008384.3:g.22874C>G

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.537C>G NP_000760.1:p.Cys179Trp
NM_000769.4:c.537C>G MANE Select NP_000760.1:p.Cys179Trp
ENST00000371321.7:c.537C>G ENSP00000360372.3:p.Cys179Trp
ENST00000464755.1:n.1300C>G ENSP00000483243.1:p.=