Canonical Allele Identifier: CA287540000
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs571789178
gnomAD v3: 17-8075399-T-C
gnomAD v4: 17-8075399-T-C
MyVariant Identifiers: chr17:g.7978717T>C (hg19) chr17:g.8075399T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075399T>C , CM000679.2:g.8075399T>C GRCh38
NC_000017.10:g.7978717T>C , CM000679.1:g.7978717T>C GRCh37
NC_000017.9:g.7919442T>C NCBI36
NG_007099.1:g.17305A>G
NG_007099.2:g.17318A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+196A>G MANE Select ENSP00000497784.1:n.1654+196A>G
ENST00000649809.1:c.718+196A>G ENSP00000496845.1:n.718+196A>G
ENST00000319144.4:c.1654+196A>G ENSP00000315167.4:n.1654+196A>G
ENST00000577351.5:n.479+776A>G
NM_001139.2:c.1654+196A>G NP_001130.1:n.1654+196A>G
NM_001139.3:c.1654+196A>G MANE Select NP_001130.1:n.1654+196A>G
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