Canonical Allele Identifier: CA2635959598

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8076550-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076555del , CM000679.2:g.8076555del	GRCh38
NC_000017.10:g.7979873del , CM000679.1:g.7979873del	GRCh37
NC_000017.9:g.7920598del	NCBI36
NG_007099.1:g.16153del
NG_007099.2:g.16166del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+106del MANE Select	ENSP00000497784.1:n.1362+106del
ENST00000649809.1:c.426+106del	ENSP00000496845.1:n.426+106del
ENST00000319144.4:c.1362+106del	ENSP00000315167.4:n.1362+106del
ENST00000577351.5:n.309+106del
ENST00000583276.5:n.746+106del
ENST00000584116.1:n.618+106del
NM_001139.2:c.1362+106del	NP_001130.1:n.1362+106del
NM_001139.3:c.1362+106del MANE Select	NP_001130.1:n.1362+106del