Canonical Allele Identifier: CA2635958315
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8075834-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075834T>C , CM000679.2:g.8075834T>C GRCh38
NC_000017.10:g.7979152T>C , CM000679.1:g.7979152T>C GRCh37
NC_000017.9:g.7919877T>C NCBI36
NG_007099.1:g.16870A>G
NG_007099.2:g.16883A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-118A>G MANE Select ENSP00000497784.1:n.1533-118A>G
ENST00000649809.1:c.597-118A>G ENSP00000496845.1:n.597-118A>G
ENST00000319144.4:c.1533-118A>G ENSP00000315167.4:n.1533-118A>G
ENST00000577351.5:n.479+341A>G
NM_001139.2:c.1533-118A>G NP_001130.1:n.1533-118A>G
NM_001139.3:c.1533-118A>G MANE Select NP_001130.1:n.1533-118A>G
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