Canonical Allele Identifier: CA934193735
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851274657

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526831A>C , CM000672.2:g.133526831A>C GRCh38
NC_000010.10:g.135340335A>C , CM000672.1:g.135340335A>C GRCh37
NC_000010.9:g.135190325A>C NCBI36
NG_008383.1:g.4469A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-82A>C ENSP00000440689.1:n.-82A>C
ENST00000541261.1:c.-82A>C ENSP00000437799.1:n.-82A>C