Canonical Allele Identifier: CA2611613578
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526889G>T , CM000672.2:g.133526889G>T GRCh38
NC_000010.10:g.135340393G>T , CM000672.1:g.135340393G>T GRCh37
NC_000010.9:g.135190383G>T NCBI36
NG_008383.1:g.4527G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+16G>T ENSP00000440689.1:n.-40+16G>T
ENST00000541261.1:c.-40+16G>T ENSP00000437799.1:n.-40+16G>T