Canonical Allele Identifier: CA8333157

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs566663426
• ExAC: 17:6900321 C / T
• gnomAD v2: 17-6900321-C-T
• gnomAD v3: 17-6997002-C-T
• gnomAD v4: 17-6997002-C-T
• MyVariant Identifiers: chr17:g.6900321C>T (hg19) ; chr17:g.6997002C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997002C>T , CM000679.2:g.6997002C>T	GRCh38
NC_000017.10:g.6900321C>T , CM000679.1:g.6900321C>T	GRCh37
NC_000017.9:g.6841045C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.312C>T (ALOX12) MANE Select	ENSP00000251535.6:p.Asp104=
ENST00000251535.10:c.312C>T (ALOX12)	ENSP00000251535.6:p.Asp104=
ENST00000480801.1:c.21C>T (ALOX12)	ENSP00000467033.1:p.Asp7=
NM_000697.2:c.312C>T (ALOX12)	NP_000688.2:p.Asp104=
NR_040089.1:n.234-11462G>A (ALOX12-AS1)
XM_011523780.1:c.669C>T (ALOX12)	XP_011522082.1:p.Asp223=
XM_011523780.2:c.669C>T (ALOX12)	XP_011522082.1:p.Asp223=
NM_000697.3:c.312C>T (ALOX12) MANE Select	NP_000688.2:p.Asp104=