Canonical Allele Identifier: CA2808396418
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086239T>G , CM000679.2:g.8086239T>G GRCh38
NC_000017.10:g.7989557T>G , CM000679.1:g.7989557T>G GRCh37
NC_000017.9:g.7930282T>G NCBI36
NG_007099.1:g.6465A>C
NG_007099.2:g.6478A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-19A>C MANE Select ENSP00000497784.1:n.148-19A>C
ENST00000319144.4:c.148-19A>C ENSP00000315167.4:n.148-19A>C
NM_001139.2:c.148-19A>C NP_001130.1:n.148-19A>C
NM_001139.3:c.148-19A>C MANE Select NP_001130.1:n.148-19A>C
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