Canonical Allele Identifier: CA1946829933
Gene: CYP2E1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532009T= , CM000672.2:g.133532009T= GRCh38
NC_000010.10:g.135345513T= , CM000672.1:g.135345513T= GRCh37
NC_000010.9:g.135195503T= NCBI36
NG_008383.1:g.9647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.488-115T= MANE Select ENSP00000252945.3:n.488-115T=
ENST00000252945.7:c.488-115T= ENSP00000252945.3:n.488-115T=
ENST00000368520.1:n.434T=
ENST00000418356.1:c.77-115T= ENSP00000397299.1:n.77-115T=
ENST00000421586.5:c.227-115T= ENSP00000412754.1:n.227-115T=
ENST00000463117.6:c.488-115T= ENSP00000440689.1:n.488-115T=
ENST00000477500.5:n.448+275T=
ENST00000480558.1:n.713-115T=
ENST00000541080.5:c.226+275T=
NM_000773.3:c.488-115T= NP_000764.1:n.488-115T=
NM_000773.4:c.488-115T= MANE Select NP_000764.1:n.488-115T=
Search 100 bp 5'
Search 100 bp 3'