Canonical Allele Identifier: CA126959
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 16897
dbSNP Id: rs4244285

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781859G>A , CM000672.2:g.94781859G>A GRCh38
NC_000010.10:g.96541616G>A , CM000672.1:g.96541616G>A GRCh37
NC_000010.9:g.96531606G>A NCBI36
NG_008384.2:g.24154G>A
NG_008384.3:g.24179G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.681G>A MANE Select ENSP00000360372.3:p.Pro227=
ENST00000645461.1:n.1734G>A
ENST00000371321.7:c.681G>A ENSP00000360372.3:p.Pro227=
ENST00000464755.1:n.1444G>A ENSP00000483243.1:p.=
NM_000769.2:c.681G>A NP_000760.1:p.Pro227=
NM_000769.4:c.681G>A MANE Select NP_000760.1:p.Pro227=