Canonical Allele Identifier: CA1946817325
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539122T= , CM000672.2:g.133539122T= GRCh38
NC_000010.10:g.135352626T= , CM000672.1:g.135352626T= GRCh37
NC_000010.9:g.135202616T= NCBI36
NG_008383.1:g.16760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*158T= MANE Select ENSP00000252945.3:n.*158T=
ENST00000368520.1:n.1358+1230T=
ENST00000463117.6:c.*158T= ENSP00000440689.1:n.*158T=
NM_000773.4:c.*158T= MANE Select NP_000764.1:n.*158T=