Canonical Allele Identifier: CA662022685
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1213675988

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527118_133527124del , CM000672.2:g.133527118_133527124del GRCh38
NC_000010.10:g.135340622_135340628del , CM000672.1:g.135340622_135340628del GRCh37
NC_000010.9:g.135190612_135190618del NCBI36
NG_008383.1:g.4756_4762del

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-239_-39-233del ENSP00000440689.1:n.-39-239_-39-233del
ENST00000541261.1:c.-39-239_-39-233del ENSP00000437799.1:n.-39-239_-39-233del