Canonical Allele Identifier: CA10652906
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 339802
dbSNP Id: rs139372063

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34788516T>C , CM000683.2:g.34788516T>C GRCh38
NC_000021.8:g.36160813T>C , CM000683.1:g.36160813T>C GRCh37
NC_000021.7:g.35082683T>C NCBI36
NG_011402.2:g.1201196A>G , LRG_482:g.1201196A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.*3619A>G MANE Select ENSP00000501943.1:n.*3619A>G
ENST00000300305.7:c.*3619A>G ENSP00000300305.3:n.*3619A>G
ENST00000344691.8:c.*3619A>G ENSP00000340690.4:n.*3619A>G
ENST00000437180.5:c.*3619A>G ENSP00000409227.1:n.*3619A>G
NM_001001890.2:c.*3619A>G NP_001001890.1:n.*3619A>G
NM_001754.4:c.*3619A>G , LRG_482t1:c.*3619A>G NP_001745.2:n.*3619A>G
XM_005261068.3:c.*3619A>G XP_005261125.1:n.*3619A>G
XM_005261069.3:c.*3619A>G XP_005261126.1:n.*3619A>G
XM_011529766.1:c.*3619A>G XP_011528068.1:n.*3619A>G
XM_011529767.1:c.*3619A>G XP_011528069.1:n.*3619A>G
XM_011529768.1:c.*3619A>G XP_011528070.1:n.*3619A>G
XM_005261069.4:c.*3619A>G XP_005261126.1:n.*3619A>G
XM_011529766.2:c.*3619A>G XP_011528068.1:n.*3619A>G
XM_011529767.2:c.*3619A>G XP_011528069.1:n.*3619A>G
XM_011529768.2:c.*3619A>G XP_011528070.1:n.*3619A>G
XM_017028487.1:c.*3619A>G XP_016883976.1:n.*3619A>G
NM_001001890.3:c.*3619A>G NP_001001890.1:n.*3619A>G
NM_001754.5:c.*3619A>G MANE Select NP_001745.2:n.*3619A>G