Canonical Allele Identifier: CA397737238
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996835T>G , CM000679.2:g.6996835T>G GRCh38
NC_000017.10:g.6900154T>G , CM000679.1:g.6900154T>G GRCh37
NC_000017.9:g.6840878T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.145T>G (ALOX12) MANE Select ENSP00000251535.6:p.Phe49Val
ENST00000251535.10:c.145T>G (ALOX12) ENSP00000251535.6:p.Phe49Val
NM_000697.2:c.145T>G (ALOX12) NP_000688.2:p.Phe49Val
NR_040089.1:n.234-11295A>C (ALOX12-AS1)
XM_011523780.1:c.502T>G (ALOX12) XP_011522082.1:p.Phe168Val
XM_011523780.2:c.502T>G (ALOX12) XP_011522082.1:p.Phe168Val
NM_000697.3:c.145T>G (ALOX12) MANE Select NP_000688.2:p.Phe49Val