Canonical Allele Identifier: CA1946817708
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1589958084

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539291T>C , CM000672.2:g.133539291T>C GRCh38
NC_000010.10:g.135352795T>C , CM000672.1:g.135352795T>C GRCh37
NC_000010.9:g.135202785T>C NCBI36
NG_008383.1:g.16929T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1399T>C