Canonical Allele Identifier: CA1929214467

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94763352T= , CM000672.2:g.94763352T=	GRCh38
NC_000010.10:g.96523109T= , CM000672.1:g.96523109T=	GRCh37
NC_000010.9:g.96513099T=	NCBI36
NG_008384.2:g.5647T=
NG_008384.3:g.5672T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.168+479T= MANE Select	ENSP00000360372.3:n.168+479T=
ENST00000371321.7:c.168+479T=	ENSP00000360372.3:n.168+479T=
ENST00000464755.1:c.932-11706T=	ENSP00000483243.1:n.932-11706T=
ENST00000480405.2:c.168+479T=	ENSP00000483847.1:n.168+479T=
NM_000769.2:c.168+479T=	NP_000760.1:n.168+479T=
NM_000769.4:c.168+479T= MANE Select	NP_000760.1:n.168+479T=