Canonical Allele Identifier: CA934180032
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1436641204

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539215T>C , CM000672.2:g.133539215T>C GRCh38
NC_000010.10:g.135352719T>C , CM000672.1:g.135352719T>C GRCh37
NC_000010.9:g.135202709T>C NCBI36
NG_008383.1:g.16853T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1323T>C