Canonical Allele Identifier: CA2246125260
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs2099798300
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075491A>G , CM000679.2:g.8075491A>G GRCh38
NC_000017.10:g.7978809A>G , CM000679.1:g.7978809A>G GRCh37
NC_000017.9:g.7919534A>G NCBI36
NG_007099.1:g.17213T>C
NG_007099.2:g.17226T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+104T>C MANE Select ENSP00000497784.1:n.1654+104T>C
ENST00000649809.1:c.718+104T>C ENSP00000496845.1:n.718+104T>C
ENST00000319144.4:c.1654+104T>C ENSP00000315167.4:n.1654+104T>C
ENST00000577351.5:n.479+684T>C
NM_001139.2:c.1654+104T>C NP_001130.1:n.1654+104T>C
NM_001139.3:c.1654+104T>C MANE Select NP_001130.1:n.1654+104T>C
Search 100 bp 5'
Search 100 bp 3'