Canonical Allele Identifier: CA216859119

Gene: CYP2E1

Linked Data

• dbSNP Id: rs9629959
• gnomAD v3: 10-133538582-G-A
• gnomAD v4: 10-133538582-G-A
• MyVariant Identifiers: chr10:g.135352086G>A (hg19) ; chr10:g.133538582G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538582G>A , CM000672.2:g.133538582G>A	GRCh38
NC_000010.10:g.135352086G>A , CM000672.1:g.135352086G>A	GRCh37
NC_000010.9:g.135202076G>A	NCBI36
NG_008383.1:g.16220G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.1298-198G>A MANE Select	ENSP00000252945.3:n.1298-198G>A
ENST00000252945.7:c.1298-198G>A	ENSP00000252945.3:n.1298-198G>A
ENST00000368520.1:n.1358+690G>A
ENST00000418356.1:c.887-198G>A	ENSP00000397299.1:n.887-198G>A
ENST00000421586.5:c.1037-198G>A	ENSP00000412754.1:n.1037-198G>A
ENST00000463117.6:c.1298-198G>A	ENSP00000440689.1:n.1298-198G>A
ENST00000469258.1:n.394-198G>A
ENST00000541080.5:c.714-198G>A
NM_000773.3:c.1298-198G>A	NP_000764.1:n.1298-198G>A
NM_000773.4:c.1298-198G>A MANE Select	NP_000764.1:n.1298-198G>A