Canonical Allele Identifier: CA1929280025

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94853055T= , CM000672.2:g.94853055T=	GRCh38
NC_000010.10:g.96612812T= , CM000672.1:g.96612812T=	GRCh37
NC_000010.9:g.96602802T=	NCBI36
NG_008384.2:g.95350T=
NG_008384.3:g.95375T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*141T= MANE Select	ENSP00000360372.3:n.*141T=
ENST00000645461.1:n.2525T=
ENST00000371321.7:c.*141T=	ENSP00000360372.3:n.*141T=
ENST00000464755.1:c.2377T=	ENSP00000483243.1:n.2377T=
NM_000769.2:c.*141T=	NP_000760.1:n.*141T=
NM_000769.4:c.*141T= MANE Select	NP_000760.1:n.*141T=