Canonical Allele Identifier: CA2611616835
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539011-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539011A>T , CM000672.2:g.133539011A>T GRCh38
NC_000010.10:g.135352515A>T , CM000672.1:g.135352515A>T GRCh37
NC_000010.9:g.135202505A>T NCBI36
NG_008383.1:g.16649A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.*47A>T MANE Select ENSP00000252945.3:n.*47A>T
ENST00000252945.7:c.*47A>T ENSP00000252945.3:n.*47A>T
ENST00000368520.1:n.1358+1119A>T
ENST00000463117.6:c.*47A>T ENSP00000440689.1:n.*47A>T
ENST00000469258.1:n.625A>T
NM_000773.3:c.*47A>T NP_000764.1:n.*47A>T
NM_000773.4:c.*47A>T MANE Select NP_000764.1:n.*47A>T
Search 100 bp 5'
Search 100 bp 3'