Canonical Allele Identifier: CA2635961945

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8086182-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086185del , CM000679.2:g.8086185del	GRCh38
NC_000017.10:g.7989503del , CM000679.1:g.7989503del	GRCh37
NC_000017.9:g.7930228del	NCBI36
NG_007099.1:g.6521del
NG_007099.2:g.6534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.185del MANE Select	ENSP00000497784.1:p.Gly62ValfsTer?
ENST00000319144.4:c.185del	ENSP00000315167.4:p.Gly62ValfsTer?
NM_001139.2:c.185del	NP_001130.1:p.Gly62ValfsTer?
NM_001139.3:c.185del MANE Select	NP_001130.1:p.Gly62ValfsTer?