Canonical Allele Identifier: CA216856360
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs932817948

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527145A>G , CM000672.2:g.133527145A>G GRCh38
NC_000010.10:g.135340649A>G , CM000672.1:g.135340649A>G GRCh37
NC_000010.9:g.135190639A>G NCBI36
NG_008383.1:g.4783A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-212A>G ENSP00000440689.1:n.-39-212A>G
ENST00000541261.1:c.-39-212A>G ENSP00000437799.1:n.-39-212A>G