Canonical Allele Identifier: CA2246126667
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs568686653
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076542C>T , CM000679.2:g.8076542C>T GRCh38
NC_000017.10:g.7979860C>T , CM000679.1:g.7979860C>T GRCh37
NC_000017.9:g.7920585C>T NCBI36
NG_007099.1:g.16162G>A
NG_007099.2:g.16175G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1362+115G>A MANE Select ENSP00000497784.1:n.1362+115G>A
ENST00000649809.1:c.426+115G>A ENSP00000496845.1:n.426+115G>A
ENST00000319144.4:c.1362+115G>A ENSP00000315167.4:n.1362+115G>A
ENST00000577351.5:n.309+115G>A
ENST00000583276.5:n.746+115G>A
ENST00000584116.1:n.618+115G>A
NM_001139.2:c.1362+115G>A NP_001130.1:n.1362+115G>A
NM_001139.3:c.1362+115G>A MANE Select NP_001130.1:n.1362+115G>A
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