Canonical Allele Identifier: CA2611613792
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527062G>C , CM000672.2:g.133527062G>C GRCh38
NC_000010.10:g.135340566G>C , CM000672.1:g.135340566G>C GRCh37
NC_000010.9:g.135190556G>C NCBI36
NG_008383.1:g.4700G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+189G>C ENSP00000440689.1:n.-40+189G>C
ENST00000541261.1:c.-40+189G>C ENSP00000437799.1:n.-40+189G>C