Canonical Allele Identifier: CA8333166
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1289083
ClinVar RCV Id: RCV001713734
dbSNP Id: rs2070589
ExAC: 17:6900362 C / T
gnomAD v2: 17-6900362-C-T
gnomAD v3: 17-6997043-C-T
gnomAD v4: 17-6997043-C-T
MyVariant Identifiers: chr17:g.6900362C>T (hg19) chr17:g.6997043C>T (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+16C>T (ALOX12) MANE Select ENSP00000251535.6:n.337+16C>T
ENST00000251535.10:c.337+16C>T (ALOX12) ENSP00000251535.6:n.337+16C>T
ENST00000480801.1:c.46+16C>T (ALOX12) ENSP00000467033.1:n.46+16C>T
NM_000697.2:c.337+16C>T (ALOX12) NP_000688.2:n.337+16C>T
NR_040089.1:n.234-11503G>A (ALOX12-AS1)
XM_011523780.1:c.694+16C>T (ALOX12) XP_011522082.1:n.694+16C>T
XM_011523780.2:c.694+16C>T (ALOX12) XP_011522082.1:n.694+16C>T
NM_000697.3:c.337+16C>T (ALOX12) MANE Select NP_000688.2:n.337+16C>T
Search 100 bp 5'
Search 100 bp 3'