Canonical Allele Identifier: CA512318669
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2146360810
MyVariant Identifiers: chr21:g.36252879G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880582G>A , CM000683.2:g.34880582G>A GRCh38
NC_000021.8:g.36252879G>A , CM000683.1:g.36252879G>A GRCh37
NC_000021.7:g.35174749G>A NCBI36
NG_011402.2:g.1109130C>T , LRG_482:g.1109130C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.483C>T MANE Select ENSP00000501943.1:p.Leu161=
ENST00000300305.7:c.483C>T ENSP00000300305.3:p.Leu161=
ENST00000344691.8:c.402C>T ENSP00000340690.4:p.Leu134=
ENST00000358356.9:c.402C>T ENSP00000351123.5:p.Leu134=
ENST00000399237.6:c.447C>T ENSP00000382182.2:p.Leu149=
ENST00000399240.5:c.402C>T ENSP00000382184.1:p.Leu134=
ENST00000437180.5:c.483C>T ENSP00000409227.1:p.Leu161=
ENST00000482318.5:c.*73C>T ENSP00000477067.1:n.*73C>T
NM_001001890.2:c.402C>T NP_001001890.1:p.Leu134=
NM_001122607.1:c.402C>T NP_001116079.1:p.Leu134=
NM_001754.4:c.483C>T , LRG_482t1:c.483C>T NP_001745.2:p.Leu161=
XM_005261068.3:c.447C>T XP_005261125.1:p.Leu149=
XM_005261069.3:c.483C>T XP_005261126.1:p.Leu161=
XM_011529766.1:c.483C>T XP_011528068.1:p.Leu161=
XM_011529767.1:c.444C>T XP_011528069.1:p.Leu148=
XM_011529768.1:c.444C>T XP_011528070.1:p.Leu148=
XM_011529770.1:c.483C>T XP_011528072.1:p.Leu161=
XR_937576.1:n.662C>T
XM_005261069.4:c.483C>T XP_005261126.1:p.Leu161=
XM_011529766.2:c.483C>T XP_011528068.1:p.Leu161=
XM_011529767.2:c.444C>T XP_011528069.1:p.Leu148=
XM_011529768.2:c.444C>T XP_011528070.1:p.Leu148=
XM_011529770.2:c.483C>T XP_011528072.1:p.Leu161=
XM_017028487.1:c.330C>T XP_016883976.1:p.Leu110=
XR_937576.2:n.709C>T
NM_001001890.3:c.402C>T NP_001001890.1:p.Leu134=
NM_001122607.2:c.402C>T NP_001116079.1:p.Leu134=
NM_001754.5:c.483C>T MANE Select NP_001745.2:p.Leu161=
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