Canonical Allele Identifier: CA470987422
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96535187G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775430G>T , CM000672.2:g.94775430G>T GRCh38
NC_000010.10:g.96535187G>T , CM000672.1:g.96535187G>T GRCh37
NC_000010.9:g.96525177G>T NCBI36
NG_008384.2:g.17725G>T
NG_008384.3:g.17750G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.372G>T MANE Select ENSP00000360372.3:p.Arg124=
ENST00000645461.1:n.1425G>T
ENST00000371321.7:c.372G>T ENSP00000360372.3:p.Arg124=
ENST00000464755.1:c.1135G>T ENSP00000483243.1:n.1135G>T
ENST00000480405.2:c.372G>T ENSP00000483847.1:p.Arg124=
NM_000769.2:c.372G>T NP_000760.1:p.Arg124=
NM_000769.4:c.372G>T MANE Select NP_000760.1:p.Arg124=