Canonical Allele Identifier: CA216856368
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs925371749

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527175C>T , CM000672.2:g.133527175C>T GRCh38
NC_000010.10:g.135340679C>T , CM000672.1:g.135340679C>T GRCh37
NC_000010.9:g.135190669C>T NCBI36
NG_008383.1:g.4813C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-39-182C>T ENSP00000440689.1:n.-39-182C>T
ENST00000541261.1:c.-39-182C>T ENSP00000437799.1:n.-39-182C>T