Canonical Allele Identifier: CA934195926

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1851344086
• gnomAD v4: 10-133532013-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532013A>G , CM000672.2:g.133532013A>G	GRCh38
NC_000010.10:g.135345517A>G , CM000672.1:g.135345517A>G	GRCh37
NC_000010.9:g.135195507A>G	NCBI36
NG_008383.1:g.9651A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.488-111A>G MANE Select	ENSP00000252945.3:n.488-111A>G
ENST00000252945.7:c.488-111A>G	ENSP00000252945.3:n.488-111A>G
ENST00000368520.1:n.438A>G
ENST00000418356.1:c.77-111A>G	ENSP00000397299.1:n.77-111A>G
ENST00000421586.5:c.227-111A>G	ENSP00000412754.1:n.227-111A>G
ENST00000463117.6:c.488-111A>G	ENSP00000440689.1:n.488-111A>G
ENST00000477500.5:n.448+279A>G
ENST00000480558.1:n.713-111A>G
ENST00000541080.5:c.226+279A>G
NM_000773.3:c.488-111A>G	NP_000764.1:n.488-111A>G
NM_000773.4:c.488-111A>G MANE Select	NP_000764.1:n.488-111A>G