Canonical Allele Identifier: CA497759435
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979645C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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