Canonical Allele Identifier: CA2635959396
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8076476-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076476G>T , CM000679.2:g.8076476G>T GRCh38
NC_000017.10:g.7979794G>T , CM000679.1:g.7979794G>T GRCh37
NC_000017.9:g.7920519G>T NCBI36
NG_007099.1:g.16228C>A
NG_007099.2:g.16241C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1363-132C>A MANE Select ENSP00000497784.1:n.1363-132C>A
ENST00000649809.1:c.427-132C>A ENSP00000496845.1:n.427-132C>A
ENST00000319144.4:c.1363-132C>A ENSP00000315167.4:n.1363-132C>A
ENST00000577351.5:n.310-132C>A
ENST00000583276.5:n.747-132C>A
ENST00000584116.1:n.619-132C>A
NM_001139.2:c.1363-132C>A NP_001130.1:n.1363-132C>A
NM_001139.3:c.1363-132C>A MANE Select NP_001130.1:n.1363-132C>A
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