Canonical Allele Identifier: CA662022684
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1290104844

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527109del , CM000672.2:g.133527109del GRCh38
NC_000010.10:g.135340613del , CM000672.1:g.135340613del GRCh37
NC_000010.9:g.135190603del NCBI36
NG_008383.1:g.4747del

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+236del ENSP00000440689.1:n.-40+236del
ENST00000541261.1:c.-40+236del ENSP00000437799.1:n.-40+236del