Canonical Allele Identifier: CA397990963
Gene: ALOX12B HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1379T>C MANE Select ENSP00000497784.1:p.Val460Ala
ENST00000649809.1:c.443T>C ENSP00000496845.1:p.Val148Ala
ENST00000319144.4:c.1379T>C ENSP00000315167.4:p.Val460Ala
ENST00000577351.5:n.326T>C
ENST00000583276.5:n.763T>C
ENST00000584116.1:n.635T>C
NM_001139.2:c.1379T>C NP_001130.1:p.Val460Ala
NM_001139.3:c.1379T>C MANE Select NP_001130.1:p.Val460Ala
Search 100 bp 5'
Search 100 bp 3'