Canonical Allele Identifier: CA981148899

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs1908484991
• gnomAD v3: 17-6997088-G-A
• gnomAD v4: 17-6997088-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997088G>A , CM000679.2:g.6997088G>A	GRCh38
NC_000017.10:g.6900407G>A , CM000679.1:g.6900407G>A	GRCh37
NC_000017.9:g.6841131G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.337+61G>A (ALOX12) MANE Select	ENSP00000251535.6:n.337+61G>A
ENST00000251535.10:c.337+61G>A (ALOX12)	ENSP00000251535.6:n.337+61G>A
ENST00000480801.1:c.46+61G>A (ALOX12)	ENSP00000467033.1:n.46+61G>A
NM_000697.2:c.337+61G>A (ALOX12)	NP_000688.2:n.337+61G>A
NR_040089.1:n.234-11548C>T (ALOX12-AS1)
XM_011523780.1:c.694+61G>A (ALOX12)	XP_011522082.1:n.694+61G>A
XM_011523780.2:c.694+61G>A (ALOX12)	XP_011522082.1:n.694+61G>A
NM_000697.3:c.337+61G>A (ALOX12) MANE Select	NP_000688.2:n.337+61G>A