Canonical Allele Identifier: CA1946817217
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539016T= , CM000672.2:g.133539016T= GRCh38
NC_000010.10:g.135352520T= , CM000672.1:g.135352520T= GRCh37
NC_000010.9:g.135202510T= NCBI36
NG_008383.1:g.16654T=

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.*52T= MANE Select ENSP00000252945.3:n.*52T=
ENST00000252945.7:c.*52T= ENSP00000252945.3:n.*52T=
ENST00000368520.1:n.1358+1124T=
ENST00000463117.6:c.*52T= ENSP00000440689.1:n.*52T=
ENST00000469258.1:n.630T=
NM_000773.3:c.*52T= NP_000764.1:n.*52T=
NM_000773.4:c.*52T= MANE Select NP_000764.1:n.*52T=