Canonical Allele Identifier: CA2246104923
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086206G= , CM000679.2:g.8086206G= GRCh38
NC_000017.10:g.7989524G= , CM000679.1:g.7989524G= GRCh37
NC_000017.9:g.7930249G= NCBI36
NG_007099.1:g.6498C=
NG_007099.2:g.6511C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.162C= MANE Select ENSP00000497784.1:p.Thr54=
ENST00000319144.4:c.162C= ENSP00000315167.4:p.Thr54=
NM_001139.2:c.162C= NP_001130.1:p.Thr54=
NM_001139.3:c.162C= MANE Select NP_001130.1:p.Thr54=