Canonical Allele Identifier: CA470833099

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96612509A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852752A>T , CM000672.2:g.94852752A>T	GRCh38
NC_000010.10:g.96612509A>T , CM000672.1:g.96612509A>T	GRCh37
NC_000010.9:g.96602499A>T	NCBI36
NG_008384.2:g.95047A>T
NG_008384.3:g.95072A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.1311A>T MANE Select	ENSP00000360372.3:p.Gly437=
ENST00000645461.1:n.2222A>T
ENST00000371321.7:c.1311A>T	ENSP00000360372.3:p.Gly437=
ENST00000464755.1:c.2074A>T	ENSP00000483243.1:n.2074A>T
NM_000769.2:c.1311A>T	NP_000760.1:p.Gly437=
NM_000769.4:c.1311A>T MANE Select	NP_000760.1:p.Gly437=