Canonical Allele Identifier: CA2246126097
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075912A= , CM000679.2:g.8075912A= GRCh38
NC_000017.10:g.7979230A= , CM000679.1:g.7979230A= GRCh37
NC_000017.9:g.7919955A= NCBI36
NG_007099.1:g.16792T=
NG_007099.2:g.16805T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-196T= MANE Select ENSP00000497784.1:n.1533-196T=
ENST00000649809.1:c.597-196T= ENSP00000496845.1:n.597-196T=
ENST00000319144.4:c.1533-196T= ENSP00000315167.4:n.1533-196T=
ENST00000577351.5:n.479+263T=
NM_001139.2:c.1533-196T= NP_001130.1:n.1533-196T=
NM_001139.3:c.1533-196T= MANE Select NP_001130.1:n.1533-196T=
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