Canonical Allele Identifier: CA662022701
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1195948710

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527154G>T , CM000672.2:g.133527154G>T GRCh38
NC_000010.10:g.135340658G>T , CM000672.1:g.135340658G>T GRCh37
NC_000010.9:g.135190648G>T NCBI36
NG_008383.1:g.4792G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-203G>T ENSP00000440689.1:n.-39-203G>T
ENST00000541261.1:c.-39-203G>T ENSP00000437799.1:n.-39-203G>T