Canonical Allele Identifier: CA1929214356

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94763244T= , CM000672.2:g.94763244T=	GRCh38
NC_000010.10:g.96523001T= , CM000672.1:g.96523001T=	GRCh37
NC_000010.9:g.96512991T=	NCBI36
NG_008384.2:g.5539T=
NG_008384.3:g.5564T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.168+371T= MANE Select	ENSP00000360372.3:n.168+371T=
ENST00000371321.7:c.168+371T=	ENSP00000360372.3:n.168+371T=
ENST00000464755.1:c.932-11814T=	ENSP00000483243.1:n.932-11814T=
ENST00000480405.2:c.168+371T=	ENSP00000483847.1:n.168+371T=
NM_000769.2:c.168+371T=	NP_000760.1:n.168+371T=
NM_000769.4:c.168+371T= MANE Select	NP_000760.1:n.168+371T=