Canonical Allele Identifier: CA377670418
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780501T>A , CM000672.2:g.94780501T>A GRCh38
NC_000010.10:g.96540258T>A , CM000672.1:g.96540258T>A GRCh37
NC_000010.9:g.96530248T>A NCBI36
NG_008384.2:g.22796T>A
NG_008384.3:g.22821T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.484T>A MANE Select ENSP00000360372.3:p.Ser162Thr
ENST00000371321.7:c.484T>A ENSP00000360372.3:p.Ser162Thr
ENST00000464755.1:n.1247T>A ENSP00000483243.1:p.=
NM_000769.2:c.484T>A NP_000760.1:p.Ser162Thr
NM_000769.4:c.484T>A MANE Select NP_000760.1:p.Ser162Thr