Canonical Allele Identifier: CA378835292
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532183A>G , CM000672.2:g.133532183A>G GRCh38
NC_000010.10:g.135345687A>G , CM000672.1:g.135345687A>G GRCh37
NC_000010.9:g.135195677A>G NCBI36
NG_008383.1:g.9821A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.547A>G MANE Select ENSP00000252945.3:p.Ile183Val
ENST00000252945.7:c.547A>G ENSP00000252945.3:p.Ile183Val
ENST00000368520.1:n.608A>G
ENST00000418356.1:c.136A>G ENSP00000397299.1:p.Ile46Val
ENST00000421586.5:c.286A>G ENSP00000412754.1:p.Ile96Val
ENST00000463117.6:c.547A>G ENSP00000440689.1:p.Ile183Val
ENST00000477500.5:n.448+449A>G
ENST00000541080.5:c.226+449A>G
NM_000773.3:c.547A>G NP_000764.1:p.Ile183Val
NM_000773.4:c.547A>G MANE Select NP_000764.1:p.Ile183Val