Canonical Allele Identifier: CA397738115
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1211423681
gnomAD v2: 17-6900301-C-T
gnomAD v4: 17-6996982-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996982C>T , CM000679.2:g.6996982C>T GRCh38
NC_000017.10:g.6900301C>T , CM000679.1:g.6900301C>T GRCh37
NC_000017.9:g.6841025C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.292C>T (ALOX12) MANE Select ENSP00000251535.6:p.Arg98Cys
ENST00000251535.10:c.292C>T (ALOX12) ENSP00000251535.6:p.Arg98Cys
ENST00000480801.1:c.1C>T (ALOX12) ENSP00000467033.1:p.Arg1Cys
NM_000697.2:c.292C>T (ALOX12) NP_000688.2:p.Arg98Cys
NR_040089.1:n.234-11442G>A (ALOX12-AS1)
XM_011523780.1:c.649C>T (ALOX12) XP_011522082.1:p.Arg217Cys
XM_011523780.2:c.649C>T (ALOX12) XP_011522082.1:p.Arg217Cys
NM_000697.3:c.292C>T (ALOX12) MANE Select NP_000688.2:p.Arg98Cys