Canonical Allele Identifier: CA8333126

Gene: ALOX12 ALOX12-AS1

Linked Data

• dbSNP Id: rs183070992
• ExAC: 17:6900116 T / C
• gnomAD v2: 17-6900116-T-C
• gnomAD v3: 17-6996797-T-C
• gnomAD v4: 17-6996797-T-C
• MyVariant Identifiers: chr17:g.6900116T>C (hg19) ; chr17:g.6996797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6996797T>C , CM000679.2:g.6996797T>C	GRCh38
NC_000017.10:g.6900116T>C , CM000679.1:g.6900116T>C	GRCh37
NC_000017.9:g.6840840T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251535.11:c.136-29T>C (ALOX12) MANE Select	ENSP00000251535.6:n.136-29T>C
ENST00000251535.10:c.136-29T>C (ALOX12)	ENSP00000251535.6:n.136-29T>C
NM_000697.2:c.136-29T>C (ALOX12)	NP_000688.2:n.136-29T>C
NR_040089.1:n.234-11257A>G (ALOX12-AS1)
XM_011523780.1:c.493-29T>C (ALOX12)	XP_011522082.1:n.493-29T>C
XM_011523780.2:c.493-29T>C (ALOX12)	XP_011522082.1:n.493-29T>C
NM_000697.3:c.136-29T>C (ALOX12) MANE Select	NP_000688.2:n.136-29T>C