Canonical Allele Identifier: CA913203336

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[94775367A>G;94781859G>A] , CM000672.2:g.[94775367A>G;94781859G>A]	GRCh38
NC_000010.10:g.[96535124A>G;96541616G>A] , CM000672.1:g.[96535124A>G;96541616G>A]	GRCh37
NC_000010.9:g.[96525114A>G;96531606G>A]	NCBI36
NG_008384.2:g.[17662A>G;24154G>A]
NG_008384.3:g.[17687A>G;24179G>A]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.[332-23A>G;681G>A] MANE Select	ENSP00000360372.3:p.Pro227=
ENST00000645461.1:n.[1385-23A>G;1734G>A]
ENST00000371321.7:c.[332-23A>G;681G>A]	ENSP00000360372.3:p.Pro227=
ENST00000464755.1:c.[1095-23A>G;1444G>A]	ENSP00000483243.1:n.[1095-23A>G;1444G>A]
NM_000769.2:c.[332-23A>G;681G>A]	NP_000760.1:p.Pro227=
NM_000769.4:c.[332-23A>G;681G>A] MANE Select	NP_000760.1:p.Pro227=