Canonical Allele Identifier: CA5616435
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs752946864

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775487C>A , CM000672.2:g.94775487C>A GRCh38
NC_000010.10:g.96535244C>A , CM000672.1:g.96535244C>A GRCh37
NC_000010.9:g.96525234C>A NCBI36
NG_008384.2:g.17782C>A
NG_008384.3:g.17807C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.429C>A MANE Select ENSP00000360372.3:p.Asp143Glu
ENST00000645461.1:n.1482C>A
ENST00000371321.7:c.429C>A ENSP00000360372.3:p.Asp143Glu
ENST00000464755.1:c.1192C>A ENSP00000483243.1:n.1192C>A
ENST00000480405.2:c.429C>A ENSP00000483847.1:p.Asp143Glu
NM_000769.2:c.429C>A NP_000760.1:p.Asp143Glu
NM_000769.4:c.429C>A MANE Select NP_000760.1:p.Asp143Glu