Canonical Allele Identifier: CA377671192
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781860G>T , CM000672.2:g.94781860G>T GRCh38
NC_000010.10:g.96541617G>T , CM000672.1:g.96541617G>T GRCh37
NC_000010.9:g.96531607G>T NCBI36
NG_008384.2:g.24155G>T
NG_008384.3:g.24180G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.682G>T MANE Select ENSP00000360372.3:p.Gly228Ter
ENST00000645461.1:n.1735G>T
ENST00000371321.7:c.682G>T ENSP00000360372.3:p.Gly228Ter
ENST00000464755.1:c.1445G>T ENSP00000483243.1:n.1445G>T
NM_000769.2:c.682G>T NP_000760.1:p.Gly228Ter
NM_000769.4:c.682G>T MANE Select NP_000760.1:p.Gly228Ter