Canonical Allele Identifier: CA2611613779
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527057G>C , CM000672.2:g.133527057G>C GRCh38
NC_000010.10:g.135340561G>C , CM000672.1:g.135340561G>C GRCh37
NC_000010.9:g.135190551G>C NCBI36
NG_008383.1:g.4695G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-40+184G>C ENSP00000440689.1:n.-40+184G>C
ENST00000541261.1:c.-40+184G>C ENSP00000437799.1:n.-40+184G>C