Canonical Allele Identifier: CA596749384
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851447682

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539207A>T , CM000672.2:g.133539207A>T GRCh38
NC_000010.10:g.135352711A>T , CM000672.1:g.135352711A>T GRCh37
NC_000010.9:g.135202701A>T NCBI36
NG_008383.1:g.16845A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1315A>T