Canonical Allele Identifier: CA497599028

Gene: ALOX12 ALOX12-AS1

Linked Data

• gnomAD v4: 17-6996894-C-T
• MyVariant Identifiers: chr17:g.6900213C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996894C>T , CM000679.2:g.6996894C>T	GRCh38
NC_000017.10:g.6900213C>T , CM000679.1:g.6900213C>T	GRCh37
NC_000017.9:g.6840937C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.204C>T (ALOX12) MANE Select	ENSP00000251535.6:p.His68=
ENST00000251535.10:c.204C>T (ALOX12)	ENSP00000251535.6:p.His68=
NM_000697.2:c.204C>T (ALOX12)	NP_000688.2:p.His68=
NR_040089.1:n.234-11354G>A (ALOX12-AS1)
XM_011523780.1:c.561C>T (ALOX12)	XP_011522082.1:p.His187=
XM_011523780.2:c.561C>T (ALOX12)	XP_011522082.1:p.His187=
NM_000697.3:c.204C>T (ALOX12) MANE Select	NP_000688.2:p.His68=