Canonical Allele Identifier: CA377669861
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775408G>T , CM000672.2:g.94775408G>T GRCh38
NC_000010.10:g.96535165G>T , CM000672.1:g.96535165G>T GRCh37
NC_000010.9:g.96525155G>T NCBI36
NG_008384.2:g.17703G>T
NG_008384.3:g.17728G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.350G>T MANE Select ENSP00000360372.3:p.Gly117Val
ENST00000645461.1:n.1403G>T
ENST00000371321.7:c.350G>T ENSP00000360372.3:p.Gly117Val
ENST00000464755.1:c.1113G>T ENSP00000483243.1:n.1113G>T
ENST00000480405.2:c.350G>T ENSP00000483847.1:p.Gly117Val
NM_000769.2:c.350G>T NP_000760.1:p.Gly117Val
NM_000769.4:c.350G>T MANE Select NP_000760.1:p.Gly117Val