Canonical Allele Identifier: CA1946821958
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526949T= , CM000672.2:g.133526949T= GRCh38
NC_000010.10:g.135340453T= , CM000672.1:g.135340453T= GRCh37
NC_000010.9:g.135190443T= NCBI36
NG_008383.1:g.4587T=

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+76T= ENSP00000440689.1:n.-40+76T=
ENST00000541261.1:c.-40+76T= ENSP00000437799.1:n.-40+76T=