Canonical Allele Identifier: CA398000011
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086186A>T , CM000679.2:g.8086186A>T GRCh38
NC_000017.10:g.7989504A>T , CM000679.1:g.7989504A>T GRCh37
NC_000017.9:g.7930229A>T NCBI36
NG_007099.1:g.6518T>A
NG_007099.2:g.6531T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.182T>A MANE Select ENSP00000497784.1:p.Leu61Gln
ENST00000319144.4:c.182T>A ENSP00000315167.4:p.Leu61Gln
NM_001139.2:c.182T>A NP_001130.1:p.Leu61Gln
NM_001139.3:c.182T>A MANE Select NP_001130.1:p.Leu61Gln