Canonical Allele Identifier: CA2635958364
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8075866-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075866G>A , CM000679.2:g.8075866G>A GRCh38
NC_000017.10:g.7979184G>A , CM000679.1:g.7979184G>A GRCh37
NC_000017.9:g.7919909G>A NCBI36
NG_007099.1:g.16838C>T
NG_007099.2:g.16851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-150C>T MANE Select ENSP00000497784.1:n.1533-150C>T
ENST00000649809.1:c.597-150C>T ENSP00000496845.1:n.597-150C>T
ENST00000319144.4:c.1533-150C>T ENSP00000315167.4:n.1533-150C>T
ENST00000577351.5:n.479+309C>T
NM_001139.2:c.1533-150C>T NP_001130.1:n.1533-150C>T
NM_001139.3:c.1533-150C>T MANE Select NP_001130.1:n.1533-150C>T
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