Canonical Allele Identifier: CA216856344
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs571910672

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527120T>C , CM000672.2:g.133527120T>C GRCh38
NC_000010.10:g.135340624T>C , CM000672.1:g.135340624T>C GRCh37
NC_000010.9:g.135190614T>C NCBI36
NG_008383.1:g.4758T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-237T>C ENSP00000440689.1:n.-39-237T>C
ENST00000541261.1:c.-39-237T>C ENSP00000437799.1:n.-39-237T>C