Canonical Allele Identifier: CA10866684
Gene: RUNX3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11249206

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24951491C>T , CM000663.2:g.24951491C>T GRCh38
NC_000001.10:g.25277982C>T , CM000663.1:g.25277982C>T GRCh37
NC_000001.9:g.25150569C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001031680.2:c.58+13023G>A VV NP_001026850.1:p.=
XM_005246024.3:c.58+13023G>A XP_005246081.1:p.=
XM_011542351.1:c.58+13023G>A XP_011540653.1:p.=
XR_947083.1:n.6391-5921C>T
XR_947086.1:n.1460+3584C>T
XR_947087.1:n.6391-8822C>T
NM_001320672.1:c.58+13023G>A VV NP_001307601.1:p.=
XM_005246024.4:c.58+13023G>A
XR_001737934.1:n.3704+3584C>T
XR_001737935.1:n.6710+3584C>T
XR_001737938.1:n.3704+3584C>T
XR_001737939.1:n.6449-5921C>T
XR_001737940.1:n.6449-8822C>T
ENST00000338888.3:c.58+13023G>A ENSP00000343477.3:p.=
ENST00000399916.5:c.58+13023G>A ENSP00000382800.1:p.=
ENST00000479341.1:n.168+13023G>A