Canonical Allele Identifier: CA512318961
Gene: RUNX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.36259341G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887044G>A , CM000683.2:g.34887044G>A GRCh38
NC_000021.8:g.36259341G>A , CM000683.1:g.36259341G>A GRCh37
NC_000021.7:g.35181211G>A NCBI36
NG_011402.2:g.1102668C>T , LRG_482:g.1102668C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.150C>T MANE Select ENSP00000501943.1:p.Gly50=
ENST00000300305.7:c.150C>T ENSP00000300305.3:p.Gly50=
ENST00000344691.8:c.69C>T ENSP00000340690.4:p.Gly23=
ENST00000358356.9:c.69C>T ENSP00000351123.5:p.Gly23=
ENST00000399237.6:c.114C>T ENSP00000382182.2:p.Gly38=
ENST00000399240.5:c.69C>T ENSP00000382184.1:p.Gly23=
ENST00000437180.5:c.150C>T ENSP00000409227.1:p.Gly50=
ENST00000455571.5:c.111C>T ENSP00000388189.1:p.Gly37=
ENST00000482318.5:c.59-6331C>T ENSP00000477067.1:n.59-6331C>T
NM_001001890.2:c.69C>T NP_001001890.1:p.Gly23=
NM_001122607.1:c.69C>T NP_001116079.1:p.Gly23=
NM_001754.4:c.150C>T , LRG_482t1:c.150C>T NP_001745.2:p.Gly50=
XM_005261068.3:c.114C>T XP_005261125.1:p.Gly38=
XM_005261069.3:c.150C>T XP_005261126.1:p.Gly50=
XM_011529766.1:c.150C>T XP_011528068.1:p.Gly50=
XM_011529767.1:c.111C>T XP_011528069.1:p.Gly37=
XM_011529768.1:c.111C>T XP_011528070.1:p.Gly37=
XM_011529770.1:c.150C>T XP_011528072.1:p.Gly50=
XR_937576.1:n.329C>T
XM_005261069.4:c.150C>T XP_005261126.1:p.Gly50=
XM_011529766.2:c.150C>T XP_011528068.1:p.Gly50=
XM_011529767.2:c.111C>T XP_011528069.1:p.Gly37=
XM_011529768.2:c.111C>T XP_011528070.1:p.Gly37=
XM_011529770.2:c.150C>T XP_011528072.1:p.Gly50=
XM_017028487.1:c.-4C>T XP_016883976.1:n.-4C>T
XR_937576.2:n.376C>T
NM_001001890.3:c.69C>T NP_001001890.1:p.Gly23=
NM_001122607.2:c.69C>T NP_001116079.1:p.Gly23=
NM_001754.5:c.150C>T MANE Select NP_001745.2:p.Gly50=
Search 100 bp 5'
Search 100 bp 3'