Canonical Allele Identifier: CA2246126711
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076626G= , CM000679.2:g.8076626G= GRCh38
NC_000017.10:g.7979944G= , CM000679.1:g.7979944G= GRCh37
NC_000017.9:g.7920669G= NCBI36
NG_007099.1:g.16078C=
NG_007099.2:g.16091C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+31C= MANE Select ENSP00000497784.1:n.1362+31C=
ENST00000649809.1:c.426+31C= ENSP00000496845.1:n.426+31C=
ENST00000319144.4:c.1362+31C= ENSP00000315167.4:n.1362+31C=
ENST00000577351.5:n.309+31C=
ENST00000583276.5:n.746+31C=
ENST00000584116.1:n.618+31C=
NM_001139.2:c.1362+31C= NP_001130.1:n.1362+31C=
NM_001139.3:c.1362+31C= MANE Select NP_001130.1:n.1362+31C=
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