Canonical Allele Identifier: CA5616488
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs373613403

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780583A>T , CM000672.2:g.94780583A>T GRCh38
NC_000010.10:g.96540340A>T , CM000672.1:g.96540340A>T GRCh37
NC_000010.9:g.96530330A>T NCBI36
NG_008384.2:g.22878A>T
NG_008384.3:g.22903A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.566A>T MANE Select ENSP00000360372.3:p.Tyr189Phe
ENST00000371321.7:c.566A>T ENSP00000360372.3:p.Tyr189Phe
ENST00000464755.1:n.1329A>T ENSP00000483243.1:p.=
NM_000769.2:c.566A>T NP_000760.1:p.Tyr189Phe
NM_000769.4:c.566A>T MANE Select NP_000760.1:p.Tyr189Phe