Canonical Allele Identifier: CA1929213696

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762734G= , CM000672.2:g.94762734G=	GRCh38
NC_000010.10:g.96522491G= , CM000672.1:g.96522491G=	GRCh37
NC_000010.9:g.96512481G=	NCBI36
NG_008384.2:g.5029G=
NG_008384.3:g.5054G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.29G= MANE Select	ENSP00000360372.3:p.Cys10=
ENST00000371321.7:c.29G=	ENSP00000360372.3:p.Cys10=
ENST00000464755.1:c.932-12324G=	ENSP00000483243.1:n.932-12324G=
ENST00000480405.2:c.29G=	ENSP00000483847.1:p.Cys10=
NM_000769.2:c.29G=	NP_000760.1:p.Cys10=
NM_000769.4:c.29G= MANE Select	NP_000760.1:p.Cys10=