Canonical Allele Identifier: CA774565144

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs1357077286
• MyVariant Identifiers: chr17:g.6899929T>C (hg19) ; chr17:g.6996610T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996610T>C , CM000679.2:g.6996610T>C	GRCh38
NC_000017.10:g.6899929T>C , CM000679.1:g.6899929T>C	GRCh37
NC_000017.9:g.6840653T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.136-216T>C (ALOX12) MANE Select	ENSP00000251535.6:n.136-216T>C
ENST00000251535.10:c.136-216T>C (ALOX12)	ENSP00000251535.6:n.136-216T>C
NM_000697.2:c.136-216T>C (ALOX12)	NP_000688.2:n.136-216T>C
NR_040089.1:n.234-11070A>G (ALOX12-AS1)
XM_011523780.1:c.493-216T>C (ALOX12)	XP_011522082.1:n.493-216T>C
XM_011523780.2:c.493-216T>C (ALOX12)	XP_011522082.1:n.493-216T>C
NM_000697.3:c.136-216T>C (ALOX12) MANE Select	NP_000688.2:n.136-216T>C