Canonical Allele Identifier: CA2611616588

Gene: CYP2E1

Linked Data

• gnomAD v4: 10-133532081-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532081C>T , CM000672.2:g.133532081C>T	GRCh38
NC_000010.10:g.135345585C>T , CM000672.1:g.135345585C>T	GRCh37
NC_000010.9:g.135195575C>T	NCBI36
NG_008383.1:g.9719C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.488-43C>T MANE Select	ENSP00000252945.3:n.488-43C>T
ENST00000252945.7:c.488-43C>T	ENSP00000252945.3:n.488-43C>T
ENST00000368520.1:n.506C>T
ENST00000418356.1:c.77-43C>T	ENSP00000397299.1:n.77-43C>T
ENST00000421586.5:c.227-43C>T	ENSP00000412754.1:n.227-43C>T
ENST00000463117.6:c.488-43C>T	ENSP00000440689.1:n.488-43C>T
ENST00000477500.5:n.448+347C>T
ENST00000480558.1:n.713-43C>T
ENST00000541080.5:c.226+347C>T
NM_000773.3:c.488-43C>T	NP_000764.1:n.488-43C>T
NM_000773.4:c.488-43C>T MANE Select	NP_000764.1:n.488-43C>T