Canonical Allele Identifier: CA19449326

Gene: RUNX3 RUNX3-AS1

Linked Data

• dbSNP Id: rs181820899
• gnomAD v2: 1-25278003-G-A
• gnomAD v3: 1-24951512-G-A
• gnomAD v4: 1-24951512-G-A
• MyVariant Identifiers: chr1:g.25278003G>A (hg19) ; chr1:g.24951512G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24951512G>A , CM000663.2:g.24951512G>A	GRCh38
NC_000001.10:g.25278003G>A , CM000663.1:g.25278003G>A	GRCh37
NC_000001.9:g.25150590G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338888.4:c.58+13002C>T (RUNX3)	ENSP00000343477.3:n.58+13002C>T
ENST00000338888.3:c.58+13002C>T (RUNX3)	ENSP00000343477.3:n.58+13002C>T
ENST00000399916.5:c.58+13002C>T (RUNX3)	ENSP00000382800.1:n.58+13002C>T
ENST00000479341.1:n.168+13002C>T (RUNX3)
NM_001031680.2:c.58+13002C>T (RUNX3)	NP_001026850.1:n.58+13002C>T
XM_005246024.3:c.58+13002C>T (RUNX3)	XP_005246081.1:n.58+13002C>T
XM_011542351.1:c.58+13002C>T (RUNX3)	XP_011540653.1:n.58+13002C>T
XR_947083.1:n.6391-5900G>A (RUNX3-AS1)
XR_947086.1:n.1460+3605G>A (RUNX3-AS1)
XR_947087.1:n.6391-8801G>A (RUNX3-AS1)
NM_001320672.1:c.58+13002C>T (RUNX3)	NP_001307601.1:n.58+13002C>T
XM_005246024.4:c.58+13002C>T (RUNX3)	XP_005246081.1:n.58+13002C>T
XR_001737934.1:n.3704+3605G>A (RUNX3-AS1)
XR_001737935.1:n.6710+3605G>A (RUNX3-AS1)
XR_001737938.1:n.3704+3605G>A (RUNX3-AS1)
XR_001737939.1:n.6449-5900G>A (RUNX3-AS1)
XR_001737940.1:n.6449-8801G>A (RUNX3-AS1)