Canonical Allele Identifier: CA981232593

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1977086857
• gnomAD v3: 17-8076559-T-C
• gnomAD v4: 17-8076559-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076559T>C , CM000679.2:g.8076559T>C	GRCh38
NC_000017.10:g.7979877T>C , CM000679.1:g.7979877T>C	GRCh37
NC_000017.9:g.7920602T>C	NCBI36
NG_007099.1:g.16145A>G
NG_007099.2:g.16158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+98A>G MANE Select	ENSP00000497784.1:n.1362+98A>G
ENST00000649809.1:c.426+98A>G	ENSP00000496845.1:n.426+98A>G
ENST00000319144.4:c.1362+98A>G	ENSP00000315167.4:n.1362+98A>G
ENST00000577351.5:n.309+98A>G
ENST00000583276.5:n.746+98A>G
ENST00000584116.1:n.618+98A>G
NM_001139.2:c.1362+98A>G	NP_001130.1:n.1362+98A>G
NM_001139.3:c.1362+98A>G MANE Select	NP_001130.1:n.1362+98A>G