Canonical Allele Identifier: CA2574724179

Gene: CYP2E1

Linked Data

• gnomAD v4: 10-133532075-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532075G>A , CM000672.2:g.133532075G>A	GRCh38
NC_000010.10:g.135345579G>A , CM000672.1:g.135345579G>A	GRCh37
NC_000010.9:g.135195569G>A	NCBI36
NG_008383.1:g.9713G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.488-49G>A MANE Select	ENSP00000252945.3:n.488-49G>A
ENST00000252945.7:c.488-49G>A	ENSP00000252945.3:n.488-49G>A
ENST00000368520.1:n.500G>A
ENST00000418356.1:c.77-49G>A	ENSP00000397299.1:n.77-49G>A
ENST00000421586.5:c.227-49G>A	ENSP00000412754.1:n.227-49G>A
ENST00000463117.6:c.488-49G>A	ENSP00000440689.1:n.488-49G>A
ENST00000477500.5:n.448+341G>A
ENST00000480558.1:n.713-49G>A
ENST00000541080.5:c.226+341G>A
NM_000773.3:c.488-49G>A	NP_000764.1:n.488-49G>A
NM_000773.4:c.488-49G>A MANE Select	NP_000764.1:n.488-49G>A