Canonical Allele Identifier: CA497759099
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1233212575
gnomAD v3: 17-8076243-A-C
gnomAD v4: 17-8076243-A-C
MyVariant Identifiers: chr17:g.7979561A>C (hg19) chr17:g.8076243A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076243A>C , CM000679.2:g.8076243A>C GRCh38
NC_000017.10:g.7979561A>C , CM000679.1:g.7979561A>C GRCh37
NC_000017.9:g.7920286A>C NCBI36
NG_007099.1:g.16461T>G
NG_007099.2:g.16474T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1464T>G MANE Select ENSP00000497784.1:p.Arg488=
ENST00000649809.1:c.528T>G ENSP00000496845.1:p.Arg176=
ENST00000319144.4:c.1464T>G ENSP00000315167.4:p.Arg488=
ENST00000577351.5:n.411T>G
ENST00000583276.5:n.848T>G
NM_001139.2:c.1464T>G NP_001130.1:p.Arg488=
NM_001139.3:c.1464T>G MANE Select NP_001130.1:p.Arg488=
Search 100 bp 5'
Search 100 bp 3'