Canonical Allele Identifier: CA662012104

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1407642932
• gnomAD v3: 10-133539198-T-G
• gnomAD v4: 10-133539198-T-G
• MyVariant Identifiers: chr10:g.135352702T>G (hg19) ; chr10:g.133539198T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133539198T>G , CM000672.2:g.133539198T>G	GRCh38
NC_000010.10:g.135352702T>G , CM000672.1:g.135352702T>G	GRCh37
NC_000010.9:g.135202692T>G	NCBI36
NG_008383.1:g.16836T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368520.1:n.1358+1306T>G