Canonical Allele Identifier: CA5616837
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs759621183

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852757G>T , CM000672.2:g.94852757G>T GRCh38
NC_000010.10:g.96612514G>T , CM000672.1:g.96612514G>T GRCh37
NC_000010.9:g.96602504G>T NCBI36
NG_008384.2:g.95052G>T
NG_008384.3:g.95077G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1316G>T MANE Select ENSP00000360372.3:p.Gly439Val
ENST00000645461.1:n.2227G>T
ENST00000371321.7:c.1316G>T ENSP00000360372.3:p.Gly439Val
ENST00000464755.1:c.2079G>T ENSP00000483243.1:n.2079G>T
NM_000769.2:c.1316G>T NP_000760.1:p.Gly439Val
NM_000769.4:c.1316G>T MANE Select NP_000760.1:p.Gly439Val