Canonical Allele Identifier: CA2576161213
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085946C>T , CM000679.2:g.8085946C>T GRCh38
NC_000017.10:g.7989264C>T , CM000679.1:g.7989264C>T GRCh37
NC_000017.9:g.7929989C>T NCBI36
NG_007099.1:g.6758G>A
NG_007099.2:g.6771G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+70G>A MANE Select ENSP00000497784.1:n.352+70G>A
ENST00000319144.4:c.352+70G>A ENSP00000315167.4:n.352+70G>A
NM_001139.2:c.352+70G>A NP_001130.1:n.352+70G>A
NM_001139.3:c.352+70G>A MANE Select NP_001130.1:n.352+70G>A
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