Canonical Allele Identifier: CA2246125540
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075614G= , CM000679.2:g.8075614G= GRCh38
NC_000017.10:g.7978932G= , CM000679.1:g.7978932G= GRCh37
NC_000017.9:g.7919657G= NCBI36
NG_007099.1:g.17090C=
NG_007099.2:g.17103C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1635C= MANE Select ENSP00000497784.1:p.Leu545=
ENST00000649809.1:c.699C= ENSP00000496845.1:p.Leu233=
ENST00000319144.4:c.1635C= ENSP00000315167.4:p.Leu545=
ENST00000577351.5:n.479+561C=
NM_001139.2:c.1635C= NP_001130.1:p.Leu545=
NM_001139.3:c.1635C= MANE Select NP_001130.1:p.Leu545=