Canonical Allele Identifier: CA2611616859
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539021-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539021G>A , CM000672.2:g.133539021G>A GRCh38
NC_000010.10:g.135352525G>A , CM000672.1:g.135352525G>A GRCh37
NC_000010.9:g.135202515G>A NCBI36
NG_008383.1:g.16659G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*57G>A MANE Select ENSP00000252945.3:n.*57G>A
ENST00000252945.7:c.*57G>A ENSP00000252945.3:n.*57G>A
ENST00000368520.1:n.1358+1129G>A
ENST00000463117.6:c.*57G>A ENSP00000440689.1:n.*57G>A
ENST00000469258.1:n.635G>A
NM_000773.3:c.*57G>A NP_000764.1:n.*57G>A
NM_000773.4:c.*57G>A MANE Select NP_000764.1:n.*57G>A
Search 100 bp 5'
Search 100 bp 3'