Canonical Allele Identifier: CA934180019
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1160250356

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539214C>G , CM000672.2:g.133539214C>G GRCh38
NC_000010.10:g.135352718C>G , CM000672.1:g.135352718C>G GRCh37
NC_000010.9:g.135202708C>G NCBI36
NG_008383.1:g.16852C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1322C>G