Canonical Allele Identifier: CA1929279997

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852986T= , CM000672.2:g.94852986T=	GRCh38
NC_000010.10:g.96612743T= , CM000672.1:g.96612743T=	GRCh37
NC_000010.9:g.96602733T=	NCBI36
NG_008384.2:g.95281T=
NG_008384.3:g.95306T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*72T= MANE Select	ENSP00000360372.3:n.*72T=
ENST00000645461.1:n.2456T=
ENST00000371321.7:c.*72T=	ENSP00000360372.3:n.*72T=
ENST00000464755.1:c.2308T=	ENSP00000483243.1:n.2308T=
NM_000769.2:c.*72T=	NP_000760.1:n.*72T=
NM_000769.4:c.*72T= MANE Select	NP_000760.1:n.*72T=