Canonical Allele Identifier: CA1946821025
Community Standard Title: NC_000010.11:g.133526101G=
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526101G= , CM000672.2:g.133526101G= GRCh38
NC_000010.10:g.135339605G= , CM000672.1:g.135339605G= GRCh37
NC_000010.9:g.135189595G= NCBI36
NG_008383.1:g.3739G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-117-695G= ENSP00000440689.1:n.-117-695G=
ENST00000541261.1:c.-118+460G= ENSP00000437799.1:n.-118+460G=
XR_001747676.2:n.705C=