Canonical Allele Identifier: CA1929221705

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780772G= , CM000672.2:g.94780772G=	GRCh38
NC_000010.10:g.96540529G= , CM000672.1:g.96540529G=	GRCh37
NC_000010.9:g.96530519G=	NCBI36
NG_008384.2:g.23067G=
NG_008384.3:g.23092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.642+113G= MANE Select	ENSP00000360372.3:n.642+113G=
ENST00000645461.1:n.1695+113G=
ENST00000371321.7:c.642+113G=	ENSP00000360372.3:n.642+113G=
ENST00000464755.1:c.1405+113G=	ENSP00000483243.1:n.1405+113G=
NM_000769.2:c.642+113G=	NP_000760.1:n.642+113G=
NM_000769.4:c.642+113G= MANE Select	NP_000760.1:n.642+113G=