Canonical Allele Identifier: CA2590217197
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs2151821902
gnomAD v3: 17-8076538-C-T
gnomAD v4: 17-8076538-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076538C>T , CM000679.2:g.8076538C>T GRCh38
NC_000017.10:g.7979856C>T , CM000679.1:g.7979856C>T GRCh37
NC_000017.9:g.7920581C>T NCBI36
NG_007099.1:g.16166G>A
NG_007099.2:g.16179G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+119G>A MANE Select ENSP00000497784.1:n.1362+119G>A
ENST00000649809.1:c.426+119G>A ENSP00000496845.1:n.426+119G>A
ENST00000319144.4:c.1362+119G>A ENSP00000315167.4:n.1362+119G>A
ENST00000577351.5:n.309+119G>A
ENST00000583276.5:n.746+119G>A
ENST00000584116.1:n.618+119G>A
NM_001139.2:c.1362+119G>A NP_001130.1:n.1362+119G>A
NM_001139.3:c.1362+119G>A MANE Select NP_001130.1:n.1362+119G>A
Search 100 bp 5'
Search 100 bp 3'