Canonical Allele Identifier: CA497600648

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs2151641078
• MyVariant Identifiers: chr17:g.6905013A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7001694A>C , CM000679.2:g.7001694A>C	GRCh38
NC_000017.10:g.6905013A>C , CM000679.1:g.6905013A>C	GRCh37
NC_000017.9:g.6845737A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.1044A>C (ALOX12) MANE Select	ENSP00000251535.6:p.Arg348=
ENST00000251535.10:c.1044A>C (ALOX12)	ENSP00000251535.6:p.Arg348=
NM_000697.2:c.1044A>C (ALOX12)	NP_000688.2:p.Arg348=
NR_040089.1:n.233+8102T>G (ALOX12-AS1)
XM_011523780.1:c.1194A>C (ALOX12)	XP_011522082.1:p.Arg398=
XM_011523780.2:c.1194A>C (ALOX12)	XP_011522082.1:p.Arg398=
NM_000697.3:c.1044A>C (ALOX12) MANE Select	NP_000688.2:p.Arg348=