Canonical Allele Identifier: CA397998942
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1598184293

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086040T>G , CM000679.2:g.8086040T>G GRCh38
NC_000017.10:g.7989358T>G , CM000679.1:g.7989358T>G GRCh37
NC_000017.9:g.7930083T>G NCBI36
NG_007099.1:g.6664A>C
NG_007099.2:g.6677A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.328A>C MANE Select ENSP00000497784.1:p.Thr110Pro
ENST00000319144.4:c.328A>C ENSP00000315167.4:p.Thr110Pro
NM_001139.2:c.328A>C NP_001130.1:p.Thr110Pro
NM_001139.3:c.328A>C MANE Select NP_001130.1:p.Thr110Pro