Canonical Allele Identifier: CA2246126465
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076331C= , CM000679.2:g.8076331C= GRCh38
NC_000017.10:g.7979649C= , CM000679.1:g.7979649C= GRCh37
NC_000017.9:g.7920374C= NCBI36
NG_007099.1:g.16373G=
NG_007099.2:g.16386G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1376G= MANE Select ENSP00000497784.1:p.Gly459=
ENST00000649809.1:c.440G= ENSP00000496845.1:p.Gly147=
ENST00000319144.4:c.1376G= ENSP00000315167.4:p.Gly459=
ENST00000577351.5:n.323G=
ENST00000583276.5:n.760G=
ENST00000584116.1:n.632G=
NM_001139.2:c.1376G= NP_001130.1:p.Gly459=
NM_001139.3:c.1376G= MANE Select NP_001130.1:p.Gly459=