Canonical Allele Identifier: CA378835232
Gene: CYP2E1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532175T>G , CM000672.2:g.133532175T>G GRCh38
NC_000010.10:g.135345679T>G , CM000672.1:g.135345679T>G GRCh37
NC_000010.9:g.135195669T>G NCBI36
NG_008383.1:g.9813T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.539T>G MANE Select ENSP00000252945.3:p.Ile180Arg
ENST00000252945.7:c.539T>G ENSP00000252945.3:p.Ile180Arg
ENST00000368520.1:n.600T>G
ENST00000418356.1:c.128T>G ENSP00000397299.1:p.Ile43Arg
ENST00000421586.5:c.278T>G ENSP00000412754.1:p.Ile93Arg
ENST00000463117.6:c.539T>G ENSP00000440689.1:p.Ile180Arg
ENST00000477500.5:n.448+441T>G
ENST00000541080.5:c.226+441T>G
NM_000773.3:c.539T>G NP_000764.1:p.Ile180Arg
NM_000773.4:c.539T>G MANE Select NP_000764.1:p.Ile180Arg