Canonical Allele Identifier: CA662022697
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1409668334

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527146A>T , CM000672.2:g.133527146A>T GRCh38
NC_000010.10:g.135340650A>T , CM000672.1:g.135340650A>T GRCh37
NC_000010.9:g.135190640A>T NCBI36
NG_008383.1:g.4784A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-211A>T ENSP00000440689.1:n.-39-211A>T
ENST00000541261.1:c.-39-211A>T ENSP00000437799.1:n.-39-211A>T