Canonical Allele Identifier: CA1946822002
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526984T= , CM000672.2:g.133526984T= GRCh38
NC_000010.10:g.135340488T= , CM000672.1:g.135340488T= GRCh37
NC_000010.9:g.135190478T= NCBI36
NG_008383.1:g.4622T=

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+111T= ENSP00000440689.1:n.-40+111T=
ENST00000541261.1:c.-40+111T= ENSP00000437799.1:n.-40+111T=