Canonical Allele Identifier: CA397737347

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs1379313179
• gnomAD v2: 17-6900169-G-A
• gnomAD v4: 17-6996850-G-A
• MyVariant Identifiers: chr17:g.6900169G>A (hg19) ; chr17:g.6996850G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996850G>A , CM000679.2:g.6996850G>A	GRCh38
NC_000017.10:g.6900169G>A , CM000679.1:g.6900169G>A	GRCh37
NC_000017.9:g.6840893G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.160G>A (ALOX12) MANE Select	ENSP00000251535.6:p.Ala54Thr
ENST00000251535.10:c.160G>A (ALOX12)	ENSP00000251535.6:p.Ala54Thr
NM_000697.2:c.160G>A (ALOX12)	NP_000688.2:p.Ala54Thr
NR_040089.1:n.234-11310C>T (ALOX12-AS1)
XM_011523780.1:c.517G>A (ALOX12)	XP_011522082.1:p.Ala173Thr
XM_011523780.2:c.517G>A (ALOX12)	XP_011522082.1:p.Ala173Thr
NM_000697.3:c.160G>A (ALOX12) MANE Select	NP_000688.2:p.Ala54Thr