Canonical Allele Identifier: CA397738045
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs755332420
gnomAD v4: 17-6996974-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996974C>T , CM000679.2:g.6996974C>T GRCh38
NC_000017.10:g.6900293C>T , CM000679.1:g.6900293C>T GRCh37
NC_000017.9:g.6841017C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.284C>T (ALOX12) MANE Select ENSP00000251535.6:p.Pro95Leu
ENST00000251535.10:c.284C>T (ALOX12) ENSP00000251535.6:p.Pro95Leu
NM_000697.2:c.284C>T (ALOX12) NP_000688.2:p.Pro95Leu
NR_040089.1:n.234-11434G>A (ALOX12-AS1)
XM_011523780.1:c.641C>T (ALOX12) XP_011522082.1:p.Pro214Leu
XM_011523780.2:c.641C>T (ALOX12) XP_011522082.1:p.Pro214Leu
NM_000697.3:c.284C>T (ALOX12) MANE Select NP_000688.2:p.Pro95Leu