Canonical Allele Identifier: CA397990966
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979646A>T (hg19) chr17:g.8076328A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076328A>T , CM000679.2:g.8076328A>T GRCh38
NC_000017.10:g.7979646A>T , CM000679.1:g.7979646A>T GRCh37
NC_000017.9:g.7920371A>T NCBI36
NG_007099.1:g.16376T>A
NG_007099.2:g.16389T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1379T>A MANE Select ENSP00000497784.1:p.Val460Glu
ENST00000649809.1:c.443T>A ENSP00000496845.1:p.Val148Glu
ENST00000319144.4:c.1379T>A ENSP00000315167.4:p.Val460Glu
ENST00000577351.5:n.326T>A
ENST00000583276.5:n.763T>A
ENST00000584116.1:n.635T>A
NM_001139.2:c.1379T>A NP_001130.1:p.Val460Glu
NM_001139.3:c.1379T>A MANE Select NP_001130.1:p.Val460Glu
Search 100 bp 5'
Search 100 bp 3'