Canonical Allele Identifier: CA2611616803
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133538991-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538991C>A , CM000672.2:g.133538991C>A GRCh38
NC_000010.10:g.135352495C>A , CM000672.1:g.135352495C>A GRCh37
NC_000010.9:g.135202485C>A NCBI36
NG_008383.1:g.16629C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*27C>A MANE Select ENSP00000252945.3:n.*27C>A
ENST00000252945.7:c.*27C>A ENSP00000252945.3:n.*27C>A
ENST00000368520.1:n.1358+1099C>A
ENST00000463117.6:c.*27C>A ENSP00000440689.1:n.*27C>A
ENST00000469258.1:n.605C>A
NM_000773.3:c.*27C>A NP_000764.1:n.*27C>A
NM_000773.4:c.*27C>A MANE Select NP_000764.1:n.*27C>A
Search 100 bp 5'
Search 100 bp 3'