Canonical Allele Identifier: CA775581103
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1371504537
gnomAD v4: 17-8075748-C-T
MyVariant Identifiers: chr17:g.7979066C>T (hg19) chr17:g.8075748C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075748C>T , CM000679.2:g.8075748C>T GRCh38
NC_000017.10:g.7979066C>T , CM000679.1:g.7979066C>T GRCh37
NC_000017.9:g.7919791C>T NCBI36
NG_007099.1:g.16956G>A
NG_007099.2:g.16969G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-32G>A MANE Select ENSP00000497784.1:n.1533-32G>A
ENST00000649809.1:c.597-32G>A ENSP00000496845.1:n.597-32G>A
ENST00000319144.4:c.1533-32G>A ENSP00000315167.4:n.1533-32G>A
ENST00000577351.5:n.479+427G>A
NM_001139.2:c.1533-32G>A NP_001130.1:n.1533-32G>A
NM_001139.3:c.1533-32G>A MANE Select NP_001130.1:n.1533-32G>A
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