Canonical Allele Identifier: CA1929213612

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762703T= , CM000672.2:g.94762703T=	GRCh38
NC_000010.10:g.96522460T= , CM000672.1:g.96522460T=	GRCh37
NC_000010.9:g.96512450T=	NCBI36
NG_008384.2:g.4998T=
NG_008384.3:g.5023T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.-3T= MANE Select	ENSP00000360372.3:n.-3T=
ENST00000371321.7:c.-3T=	ENSP00000360372.3:n.-3T=
ENST00000464755.1:c.932-12355T=	ENSP00000483243.1:n.932-12355T=
ENST00000480405.2:c.-3T=	ENSP00000483847.1:n.-3T=
NM_000769.2:c.-3T=	NP_000760.1:n.-3T=
NM_000769.4:c.-3T= MANE Select	NP_000760.1:n.-3T=