Canonical Allele Identifier: CA2611616856
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539020A>G , CM000672.2:g.133539020A>G GRCh38
NC_000010.10:g.135352524A>G , CM000672.1:g.135352524A>G GRCh37
NC_000010.9:g.135202514A>G NCBI36
NG_008383.1:g.16658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*56A>G MANE Select ENSP00000252945.3:n.*56A>G
ENST00000252945.7:c.*56A>G ENSP00000252945.3:n.*56A>G
ENST00000368520.1:n.1358+1128A>G
ENST00000463117.6:c.*56A>G ENSP00000440689.1:n.*56A>G
ENST00000469258.1:n.634A>G
NM_000773.3:c.*56A>G NP_000764.1:n.*56A>G
NM_000773.4:c.*56A>G MANE Select NP_000764.1:n.*56A>G