Canonical Allele Identifier: CA2576161039

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8076350-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076352del , CM000679.2:g.8076352del	GRCh38
NC_000017.10:g.7979670del , CM000679.1:g.7979670del	GRCh37
NC_000017.9:g.7920395del	NCBI36
NG_007099.1:g.16353del
NG_007099.2:g.16366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1363-7del MANE Select	ENSP00000497784.1:n.1363-7del
ENST00000649809.1:c.427-7del	ENSP00000496845.1:n.427-7del
ENST00000319144.4:c.1363-7del	ENSP00000315167.4:n.1363-7del
ENST00000577351.5:n.310-7del
ENST00000583276.5:n.747-7del
ENST00000584116.1:n.619-7del
NM_001139.2:c.1363-7del	NP_001130.1:n.1363-7del
NM_001139.3:c.1363-7del MANE Select	NP_001130.1:n.1363-7del