Canonical Allele Identifier: CA8333378

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs759913750
• ExAC: 17:6904908 C / A
• gnomAD v2: 17-6904908-C-A
• gnomAD v4: 17-7001589-C-A
• MyVariant Identifiers: chr17:g.6904908C>A (hg19) ; chr17:g.7001589C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001589C>A , CM000679.2:g.7001589C>A	GRCh38
NC_000017.10:g.6904908C>A , CM000679.1:g.6904908C>A	GRCh37
NC_000017.9:g.6845632C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.952-13C>A (ALOX12) MANE Select	ENSP00000251535.6:n.952-13C>A
ENST00000251535.10:c.952-13C>A (ALOX12)	ENSP00000251535.6:n.952-13C>A
NM_000697.2:c.952-13C>A (ALOX12)	NP_000688.2:n.952-13C>A
NR_040089.1:n.233+8207G>T (ALOX12-AS1)
XM_011523780.1:c.1102-13C>A (ALOX12)	XP_011522082.1:n.1102-13C>A
XM_011523780.2:c.1102-13C>A (ALOX12)	XP_011522082.1:n.1102-13C>A
NM_000697.3:c.952-13C>A (ALOX12) MANE Select	NP_000688.2:n.952-13C>A