Canonical Allele Identifier: CA512319000
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834488
ClinVar RCV Id: RCV003630615
MyVariant Identifiers: chr21:g.36259389G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887092G>T , CM000683.2:g.34887092G>T GRCh38
NC_000021.8:g.36259389G>T , CM000683.1:g.36259389G>T GRCh37
NC_000021.7:g.35181259G>T NCBI36
NG_011402.2:g.1102620C>A , LRG_482:g.1102620C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.102C>A MANE Select ENSP00000501943.1:p.Ala34=
ENST00000300305.7:c.102C>A ENSP00000300305.3:p.Ala34=
ENST00000344691.8:c.21C>A ENSP00000340690.4:p.Ala7=
ENST00000358356.9:c.21C>A ENSP00000351123.5:p.Ala7=
ENST00000399237.6:c.66C>A ENSP00000382182.2:p.Ala22=
ENST00000399240.5:c.21C>A ENSP00000382184.1:p.Ala7=
ENST00000437180.5:c.102C>A ENSP00000409227.1:p.Ala34=
ENST00000455571.5:c.63C>A ENSP00000388189.1:p.Ala21=
ENST00000475045.6:c.102C>A ENSP00000477072.1:p.Ala34=
ENST00000482318.5:c.59-6379C>A ENSP00000477067.1:n.59-6379C>A
NM_001001890.2:c.21C>A NP_001001890.1:p.Ala7=
NM_001122607.1:c.21C>A NP_001116079.1:p.Ala7=
NM_001754.4:c.102C>A , LRG_482t1:c.102C>A NP_001745.2:p.Ala34=
XM_005261068.3:c.66C>A XP_005261125.1:p.Ala22=
XM_005261069.3:c.102C>A XP_005261126.1:p.Ala34=
XM_011529766.1:c.102C>A XP_011528068.1:p.Ala34=
XM_011529767.1:c.63C>A XP_011528069.1:p.Ala21=
XM_011529768.1:c.63C>A XP_011528070.1:p.Ala21=
XM_011529770.1:c.102C>A XP_011528072.1:p.Ala34=
XR_937576.1:n.281C>A
XM_005261069.4:c.102C>A XP_005261126.1:p.Ala34=
XM_011529766.2:c.102C>A XP_011528068.1:p.Ala34=
XM_011529767.2:c.63C>A XP_011528069.1:p.Ala21=
XM_011529768.2:c.63C>A XP_011528070.1:p.Ala21=
XM_011529770.2:c.102C>A XP_011528072.1:p.Ala34=
XM_017028487.1:c.-52C>A XP_016883976.1:n.-52C>A
XR_937576.2:n.328C>A
NM_001001890.3:c.21C>A NP_001001890.1:p.Ala7=
NM_001122607.2:c.21C>A NP_001116079.1:p.Ala7=
NM_001754.5:c.102C>A MANE Select NP_001745.2:p.Ala34=
Search 100 bp 5'
Search 100 bp 3'