Canonical Allele Identifier: CA999691313
Gene: RUNX3 HGNC NCBI
RUNX3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1641767402
gnomAD v3: 1-24951573-C-A
gnomAD v4: 1-24951573-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24951573C>A , CM000663.2:g.24951573C>A GRCh38
NC_000001.10:g.25278064C>A , CM000663.1:g.25278064C>A GRCh37
NC_000001.9:g.25150651C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000338888.4:c.58+12941G>T (RUNX3) ENSP00000343477.3:n.58+12941G>T
ENST00000338888.3:c.58+12941G>T (RUNX3) ENSP00000343477.3:n.58+12941G>T
ENST00000399916.5:c.58+12941G>T (RUNX3) ENSP00000382800.1:n.58+12941G>T
ENST00000479341.1:n.168+12941G>T (RUNX3)
NM_001031680.2:c.58+12941G>T (RUNX3) NP_001026850.1:n.58+12941G>T
XM_005246024.3:c.58+12941G>T (RUNX3) XP_005246081.1:n.58+12941G>T
XM_011542351.1:c.58+12941G>T (RUNX3) XP_011540653.1:n.58+12941G>T
XR_947083.1:n.6391-5839C>A (RUNX3-AS1)
XR_947086.1:n.1460+3666C>A (RUNX3-AS1)
XR_947087.1:n.6391-8740C>A (RUNX3-AS1)
NM_001320672.1:c.58+12941G>T (RUNX3) NP_001307601.1:n.58+12941G>T
XM_005246024.4:c.58+12941G>T (RUNX3) XP_005246081.1:n.58+12941G>T
XR_001737934.1:n.3704+3666C>A (RUNX3-AS1)
XR_001737935.1:n.6710+3666C>A (RUNX3-AS1)
XR_001737938.1:n.3704+3666C>A (RUNX3-AS1)
XR_001737939.1:n.6449-5839C>A (RUNX3-AS1)
XR_001737940.1:n.6449-8740C>A (RUNX3-AS1)