Canonical Allele Identifier: CA934178938
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851437679
gnomAD v3: 10-133538747-T-A
gnomAD v4: 10-133538747-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538747T>A , CM000672.2:g.133538747T>A GRCh38
NC_000010.10:g.135352251T>A , CM000672.1:g.135352251T>A GRCh37
NC_000010.9:g.135202241T>A NCBI36
NG_008383.1:g.16385T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1298-33T>A MANE Select ENSP00000252945.3:n.1298-33T>A
ENST00000252945.7:c.1298-33T>A ENSP00000252945.3:n.1298-33T>A
ENST00000368520.1:n.1358+855T>A
ENST00000418356.1:c.887-33T>A ENSP00000397299.1:n.887-33T>A
ENST00000421586.5:c.1037-33T>A ENSP00000412754.1:n.1037-33T>A
ENST00000463117.6:c.1298-33T>A ENSP00000440689.1:n.1298-33T>A
ENST00000469258.1:n.394-33T>A
ENST00000541080.5:c.714-33T>A
NM_000773.3:c.1298-33T>A NP_000764.1:n.1298-33T>A
NM_000773.4:c.1298-33T>A MANE Select NP_000764.1:n.1298-33T>A
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