Canonical Allele Identifier: CA2611616433

Gene: CYP2E1

Linked Data

• gnomAD v4: 10-133531989-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133531989A>T , CM000672.2:g.133531989A>T	GRCh38
NC_000010.10:g.135345493A>T , CM000672.1:g.135345493A>T	GRCh37
NC_000010.9:g.135195483A>T	NCBI36
NG_008383.1:g.9627A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.488-135A>T MANE Select	ENSP00000252945.3:n.488-135A>T
ENST00000252945.7:c.488-135A>T	ENSP00000252945.3:n.488-135A>T
ENST00000368520.1:n.414A>T
ENST00000418356.1:c.77-135A>T	ENSP00000397299.1:n.77-135A>T
ENST00000421586.5:c.227-135A>T	ENSP00000412754.1:n.227-135A>T
ENST00000463117.6:c.488-135A>T	ENSP00000440689.1:n.488-135A>T
ENST00000477500.5:n.448+255A>T
ENST00000480558.1:n.713-135A>T
ENST00000541080.5:c.226+255A>T
NM_000773.3:c.488-135A>T	NP_000764.1:n.488-135A>T
NM_000773.4:c.488-135A>T MANE Select	NP_000764.1:n.488-135A>T