Canonical Allele Identifier: CA981148904

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs1908486459
• gnomAD v3: 17-6997118-T-G
• gnomAD v4: 17-6997118-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997118T>G , CM000679.2:g.6997118T>G	GRCh38
NC_000017.10:g.6900437T>G , CM000679.1:g.6900437T>G	GRCh37
NC_000017.9:g.6841161T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.337+91T>G (ALOX12) MANE Select	ENSP00000251535.6:n.337+91T>G
ENST00000251535.10:c.337+91T>G (ALOX12)	ENSP00000251535.6:n.337+91T>G
ENST00000480801.1:c.46+91T>G (ALOX12)	ENSP00000467033.1:n.46+91T>G
NM_000697.2:c.337+91T>G (ALOX12)	NP_000688.2:n.337+91T>G
NR_040089.1:n.234-11578A>C (ALOX12-AS1)
XM_011523780.1:c.694+91T>G (ALOX12)	XP_011522082.1:n.694+91T>G
XM_011523780.2:c.694+91T>G (ALOX12)	XP_011522082.1:n.694+91T>G
NM_000697.3:c.337+91T>G (ALOX12) MANE Select	NP_000688.2:n.337+91T>G