Canonical Allele Identifier: CA2611616854
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539019-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539019G>A , CM000672.2:g.133539019G>A GRCh38
NC_000010.10:g.135352523G>A , CM000672.1:g.135352523G>A GRCh37
NC_000010.9:g.135202513G>A NCBI36
NG_008383.1:g.16657G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*55G>A MANE Select ENSP00000252945.3:n.*55G>A
ENST00000252945.7:c.*55G>A ENSP00000252945.3:n.*55G>A
ENST00000368520.1:n.1358+1127G>A
ENST00000463117.6:c.*55G>A ENSP00000440689.1:n.*55G>A
ENST00000469258.1:n.633G>A
NM_000773.3:c.*55G>A NP_000764.1:n.*55G>A
NM_000773.4:c.*55G>A MANE Select NP_000764.1:n.*55G>A
Search 100 bp 5'
Search 100 bp 3'