Canonical Allele Identifier: CA1929278214

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94849877C= , CM000672.2:g.94849877C=	GRCh38
NC_000010.10:g.96609634C= , CM000672.1:g.96609634C=	GRCh37
NC_000010.9:g.96599624C=	NCBI36
NG_008384.2:g.92172C=
NG_008384.3:g.92197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1150-40C= MANE Select	ENSP00000360372.3:n.1150-40C=
ENST00000645461.1:n.2061-40C=
ENST00000371321.7:c.1150-40C=	ENSP00000360372.3:n.1150-40C=
ENST00000464755.1:c.1913-40C=	ENSP00000483243.1:n.1913-40C=
NM_000769.2:c.1150-40C=	NP_000760.1:n.1150-40C=
NM_000769.4:c.1150-40C= MANE Select	NP_000760.1:n.1150-40C=