Canonical Allele Identifier: CA2246126698
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076586C= , CM000679.2:g.8076586C= GRCh38
NC_000017.10:g.7979904C= , CM000679.1:g.7979904C= GRCh37
NC_000017.9:g.7920629C= NCBI36
NG_007099.1:g.16118G=
NG_007099.2:g.16131G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+71G= MANE Select ENSP00000497784.1:n.1362+71G=
ENST00000649809.1:c.426+71G= ENSP00000496845.1:n.426+71G=
ENST00000319144.4:c.1362+71G= ENSP00000315167.4:n.1362+71G=
ENST00000577351.5:n.309+71G=
ENST00000583276.5:n.746+71G=
ENST00000584116.1:n.618+71G=
NM_001139.2:c.1362+71G= NP_001130.1:n.1362+71G=
NM_001139.3:c.1362+71G= MANE Select NP_001130.1:n.1362+71G=
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