Canonical Allele Identifier: CA2611616851
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539016-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539016T>A , CM000672.2:g.133539016T>A GRCh38
NC_000010.10:g.135352520T>A , CM000672.1:g.135352520T>A GRCh37
NC_000010.9:g.135202510T>A NCBI36
NG_008383.1:g.16654T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.*52T>A MANE Select ENSP00000252945.3:n.*52T>A
ENST00000252945.7:c.*52T>A ENSP00000252945.3:n.*52T>A
ENST00000368520.1:n.1358+1124T>A
ENST00000463117.6:c.*52T>A ENSP00000440689.1:n.*52T>A
ENST00000469258.1:n.630T>A
NM_000773.3:c.*52T>A NP_000764.1:n.*52T>A
NM_000773.4:c.*52T>A MANE Select NP_000764.1:n.*52T>A
Search 100 bp 5'
Search 100 bp 3'