Canonical Allele Identifier: CA2246126713
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076629T= , CM000679.2:g.8076629T= GRCh38
NC_000017.10:g.7979947T= , CM000679.1:g.7979947T= GRCh37
NC_000017.9:g.7920672T= NCBI36
NG_007099.1:g.16075A=
NG_007099.2:g.16088A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+28A= MANE Select ENSP00000497784.1:n.1362+28A=
ENST00000649809.1:c.426+28A= ENSP00000496845.1:n.426+28A=
ENST00000319144.4:c.1362+28A= ENSP00000315167.4:n.1362+28A=
ENST00000577351.5:n.309+28A=
ENST00000583276.5:n.746+28A=
ENST00000584116.1:n.618+28A=
NM_001139.2:c.1362+28A= NP_001130.1:n.1362+28A=
NM_001139.3:c.1362+28A= MANE Select NP_001130.1:n.1362+28A=
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