Canonical Allele Identifier: CA2635962080
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8086239-T-A
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Genomic Alleles

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

Transcript Alleles

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