Canonical Allele Identifier: CA774565503

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs2070589
• gnomAD v4: 17-6997043-C-G
• MyVariant Identifiers: chr17:g.6900362C>G (hg19) ; chr17:g.6997043C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6997043C>G , CM000679.2:g.6997043C>G	GRCh38
NC_000017.10:g.6900362C>G , CM000679.1:g.6900362C>G	GRCh37
NC_000017.9:g.6841086C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.337+16C>G (ALOX12) MANE Select	ENSP00000251535.6:n.337+16C>G
ENST00000251535.10:c.337+16C>G (ALOX12)	ENSP00000251535.6:n.337+16C>G
ENST00000480801.1:c.46+16C>G (ALOX12)	ENSP00000467033.1:n.46+16C>G
NM_000697.2:c.337+16C>G (ALOX12)	NP_000688.2:n.337+16C>G
NR_040089.1:n.234-11503G>C (ALOX12-AS1)
XM_011523780.1:c.694+16C>G (ALOX12)	XP_011522082.1:n.694+16C>G
XM_011523780.2:c.694+16C>G (ALOX12)	XP_011522082.1:n.694+16C>G
NM_000697.3:c.337+16C>G (ALOX12) MANE Select	NP_000688.2:n.337+16C>G