Canonical Allele Identifier: CA497759439
Gene: ALOX12B HGNC NCBI

Linked Data

COSMIC: COSM5387664 COSM5387665
MyVariant Identifiers: chr17:g.7979645C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076327C>T , CM000679.2:g.8076327C>T GRCh38
NC_000017.10:g.7979645C>T , CM000679.1:g.7979645C>T GRCh37
NC_000017.9:g.7920370C>T NCBI36
NG_007099.1:g.16377G>A
NG_007099.2:g.16390G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1380G>A MANE Select ENSP00000497784.1:p.Val460=
ENST00000649809.1:c.444G>A ENSP00000496845.1:p.Val148=
ENST00000319144.4:c.1380G>A ENSP00000315167.4:p.Val460=
ENST00000577351.5:n.327G>A
ENST00000583276.5:n.764G>A
ENST00000584116.1:n.636G>A
NM_001139.2:c.1380G>A NP_001130.1:p.Val460=
NM_001139.3:c.1380G>A MANE Select NP_001130.1:p.Val460=
Search 100 bp 5'
Search 100 bp 3'