Canonical Allele Identifier: CA10665290
Gene: RUNX3 HGNC NCBI
RUNX3-AS1 HGNC NCBI
COSMIC:
COSN6451157 (not active)
MyVariant.info:
GRCh38 chr1:g.24946709T>C
GRCh37 chr1:g.25273200T>C
gnomAD v2:
1:25273200 T / C
gnomAD v3:
1:24946709 T / C
gnomAD v4:
chr1-24946709-T-C
Joint Max Group AF 0.53735771 (AMR)
Genomes Max Group AF 0.53735771 (AMR)
dbSNP:
7551188
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24946709T>C , CM000663.2:g.24946709T>C GRCh38
NC_000001.10:g.25273200T>C , CM000663.1:g.25273200T>C GRCh37
NC_000001.9:g.25145787T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338888.4:c.59-16857A>G (RUNX3) ENSP00000343477.3:n.59-16857A>G
ENST00000338888.3:c.59-16857A>G (RUNX3) ENSP00000343477.3:n.59-16857A>G
ENST00000399916.5:c.59-16857A>G (RUNX3) ENSP00000382800.1:n.59-16857A>G
ENST00000479341.1:n.169-16857A>G (RUNX3)
NM_001031680.2:c.59-16857A>G (RUNX3) NP_001026850.1:n.59-16857A>G
XM_005246024.3:c.59-16857A>G (RUNX3) XP_005246081.1:n.59-16857A>G
XM_011542351.1:c.59-16857A>G (RUNX3) XP_011540653.1:n.59-16857A>G
XR_947083.1:n.6390+7808T>C (RUNX3-AS1)
XR_947086.1:n.262T>C (RUNX3-AS1)
XR_947087.1:n.6390+7808T>C (RUNX3-AS1)
NM_001320672.1:c.59-16857A>G (RUNX3) NP_001307601.1:n.59-16857A>G
XM_005246024.4:c.59-16857A>G (RUNX3) XP_005246081.1:n.59-16857A>G
XR_001737934.1:n.2506T>C (RUNX3-AS1)
XR_001737935.1:n.6449-937T>C (RUNX3-AS1)
XR_001737938.1:n.2506T>C (RUNX3-AS1)
XR_001737939.1:n.6448+7808T>C (RUNX3-AS1)
XR_001737940.1:n.6448+7808T>C (RUNX3-AS1)
Search 100 bp 5'
Search 100 bp 3'