Canonical Allele Identifier: CA8333251
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6998976G>A , CM000679.2:g.6998976G>A GRCh38
NC_000017.10:g.6902295G>A , CM000679.1:g.6902295G>A GRCh37
NC_000017.9:g.6843019G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.566G>A (ALOX12) MANE Select ENSP00000251535.6:p.Arg189His
ENST00000251535.10:c.566G>A (ALOX12) ENSP00000251535.6:p.Arg189His
ENST00000480801.1:c.251+139G>A (ALOX12) ENSP00000467033.1:n.251+139G>A
NM_000697.2:c.566G>A (ALOX12) NP_000688.2:p.Arg189His
NR_040089.1:n.233+10820C>T (ALOX12-AS1)
XM_011523780.1:c.899+139G>A (ALOX12) XP_011522082.1:n.899+139G>A
XM_011523780.2:c.899+139G>A (ALOX12) XP_011522082.1:n.899+139G>A
NM_000697.3:c.566G>A (ALOX12) MANE Select NP_000688.2:p.Arg189His