Canonical Allele Identifier: CA470987313

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96534925G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775168G>A , CM000672.2:g.94775168G>A	GRCh38
NC_000010.10:g.96534925G>A , CM000672.1:g.96534925G>A	GRCh37
NC_000010.9:g.96524915G>A	NCBI36
NG_008384.2:g.17463G>A
NG_008384.3:g.17488G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.279G>A MANE Select	ENSP00000360372.3:p.Glu93=
ENST00000645461.1:n.1332G>A
ENST00000371321.7:c.279G>A	ENSP00000360372.3:p.Glu93=
ENST00000464755.1:c.1042G>A	ENSP00000483243.1:n.1042G>A
ENST00000480405.2:c.279G>A	ENSP00000483847.1:p.Glu93=
NM_000769.2:c.279G>A	NP_000760.1:p.Glu93=
NM_000769.4:c.279G>A MANE Select	NP_000760.1:p.Glu93=