Canonical Allele Identifier: CA1946817298
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539101A= , CM000672.2:g.133539101A= GRCh38
NC_000010.10:g.135352605A= , CM000672.1:g.135352605A= GRCh37
NC_000010.9:g.135202595A= NCBI36
NG_008383.1:g.16739A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*137A= MANE Select ENSP00000252945.3:n.*137A=
ENST00000252945.7:c.*137A= ENSP00000252945.3:n.*137A=
ENST00000368520.1:n.1358+1209A=
ENST00000463117.6:c.*137A= ENSP00000440689.1:n.*137A=
ENST00000469258.1:n.715A=
NM_000773.3:c.*137A= NP_000764.1:n.*137A=
NM_000773.4:c.*137A= MANE Select NP_000764.1:n.*137A=