Canonical Allele Identifier: CA2733190610

Gene: ALOX12B

Linked Data

• dbSNP Id: rs2151821677

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075760del , CM000679.2:g.8075760del	GRCh38
NC_000017.10:g.7979078del , CM000679.1:g.7979078del	GRCh37
NC_000017.9:g.7919803del	NCBI36
NG_007099.1:g.16946del
NG_007099.2:g.16959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1533-42del MANE Select	ENSP00000497784.1:n.1533-42del
ENST00000649809.1:c.597-42del	ENSP00000496845.1:n.597-42del
ENST00000319144.4:c.1533-42del	ENSP00000315167.4:n.1533-42del
ENST00000577351.5:n.479+417del
NM_001139.2:c.1533-42del	NP_001130.1:n.1533-42del
NM_001139.3:c.1533-42del MANE Select	NP_001130.1:n.1533-42del