Canonical Allele Identifier: CA397999713
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086132T>G , CM000679.2:g.8086132T>G GRCh38
NC_000017.10:g.7989450T>G , CM000679.1:g.7989450T>G GRCh37
NC_000017.9:g.7930175T>G NCBI36
NG_007099.1:g.6572A>C
NG_007099.2:g.6585A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.236A>C MANE Select ENSP00000497784.1:p.Lys79Thr
ENST00000319144.4:c.236A>C ENSP00000315167.4:p.Lys79Thr
NM_001139.2:c.236A>C NP_001130.1:p.Lys79Thr
NM_001139.3:c.236A>C MANE Select NP_001130.1:p.Lys79Thr