Canonical Allele Identifier: CA2635958343
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8075860-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075860G>C , CM000679.2:g.8075860G>C GRCh38
NC_000017.10:g.7979178G>C , CM000679.1:g.7979178G>C GRCh37
NC_000017.9:g.7919903G>C NCBI36
NG_007099.1:g.16844C>G
NG_007099.2:g.16857C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-144C>G MANE Select ENSP00000497784.1:n.1533-144C>G
ENST00000649809.1:c.597-144C>G ENSP00000496845.1:n.597-144C>G
ENST00000319144.4:c.1533-144C>G ENSP00000315167.4:n.1533-144C>G
ENST00000577351.5:n.479+315C>G
NM_001139.2:c.1533-144C>G NP_001130.1:n.1533-144C>G
NM_001139.3:c.1533-144C>G MANE Select NP_001130.1:n.1533-144C>G
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