Canonical Allele Identifier: CA470987342

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96535154T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775397T>G , CM000672.2:g.94775397T>G	GRCh38
NC_000010.10:g.96535154T>G , CM000672.1:g.96535154T>G	GRCh37
NC_000010.9:g.96525144T>G	NCBI36
NG_008384.2:g.17692T>G
NG_008384.3:g.17717T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.339T>G MANE Select	ENSP00000360372.3:p.Val113=
ENST00000645461.1:n.1392T>G
ENST00000371321.7:c.339T>G	ENSP00000360372.3:p.Val113=
ENST00000464755.1:c.1102T>G	ENSP00000483243.1:n.1102T>G
ENST00000480405.2:c.339T>G	ENSP00000483847.1:p.Val113=
NM_000769.2:c.339T>G	NP_000760.1:p.Val113=
NM_000769.4:c.339T>G MANE Select	NP_000760.1:p.Val113=