Canonical Allele Identifier: CA2576161012

Gene: ALOX12B

Linked Data

• dbSNP Id: rs2151821600
• gnomAD v4: 17-8075566-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075567_8075568del , CM000679.2:g.8075567_8075568del	GRCh38
NC_000017.10:g.7978885_7978886del , CM000679.1:g.7978885_7978886del	GRCh37
NC_000017.9:g.7919610_7919611del	NCBI36
NG_007099.1:g.17136_17137del
NG_007099.2:g.17149_17150del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1654+27_1654+28del MANE Select	ENSP00000497784.1:n.1654+27_1654+28del
ENST00000649809.1:c.718+27_718+28del	ENSP00000496845.1:n.718+27_718+28del
ENST00000319144.4:c.1654+27_1654+28del	ENSP00000315167.4:n.1654+27_1654+28del
ENST00000577351.5:n.479+607_479+608del
NM_001139.2:c.1654+27_1654+28del	NP_001130.1:n.1654+27_1654+28del
NM_001139.3:c.1654+27_1654+28del MANE Select	NP_001130.1:n.1654+27_1654+28del