Canonical Allele Identifier: CA397989922
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7978993G>C (hg19) chr17:g.8075675G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075675G>C , CM000679.2:g.8075675G>C GRCh38
NC_000017.10:g.7978993G>C , CM000679.1:g.7978993G>C GRCh37
NC_000017.9:g.7919718G>C NCBI36
NG_007099.1:g.17029C>G
NG_007099.2:g.17042C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1574C>G MANE Select ENSP00000497784.1:p.Ala525Gly
ENST00000649809.1:c.638C>G ENSP00000496845.1:p.Ala213Gly
ENST00000319144.4:c.1574C>G ENSP00000315167.4:p.Ala525Gly
ENST00000577351.5:n.479+500C>G
NM_001139.2:c.1574C>G NP_001130.1:p.Ala525Gly
NM_001139.3:c.1574C>G MANE Select NP_001130.1:p.Ala525Gly
Search 100 bp 5'
Search 100 bp 3'