Canonical Allele Identifier: CA1929214462

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94763351G= , CM000672.2:g.94763351G=	GRCh38
NC_000010.10:g.96523108G= , CM000672.1:g.96523108G=	GRCh37
NC_000010.9:g.96513098G=	NCBI36
NG_008384.2:g.5646G=
NG_008384.3:g.5671G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.168+478G= MANE Select	ENSP00000360372.3:n.168+478G=
ENST00000371321.7:c.168+478G=	ENSP00000360372.3:n.168+478G=
ENST00000464755.1:c.932-11707G=	ENSP00000483243.1:n.932-11707G=
ENST00000480405.2:c.168+478G=	ENSP00000483847.1:n.168+478G=
NM_000769.2:c.168+478G=	NP_000760.1:n.168+478G=
NM_000769.4:c.168+478G= MANE Select	NP_000760.1:n.168+478G=