Canonical Allele Identifier: CA2589253038
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851448084

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539230T>A , CM000672.2:g.133539230T>A GRCh38
NC_000010.10:g.135352734T>A , CM000672.1:g.135352734T>A GRCh37
NC_000010.9:g.135202724T>A NCBI36
NG_008383.1:g.16868T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1338T>A