Canonical Allele Identifier: CA10014597
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs751439026
ExAC: 21:36259420 C / A
gnomAD v2: 21-36259420-C-A
gnomAD v3: 21-34887123-C-A
gnomAD v4: 21-34887123-C-A
MyVariant Identifiers: chr21:g.36259420C>A (hg19) chr21:g.34887123C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887123C>A , CM000683.2:g.34887123C>A GRCh38
NC_000021.8:g.36259420C>A , CM000683.1:g.36259420C>A GRCh37
NC_000021.7:g.35181290C>A NCBI36
NG_011402.2:g.1102589G>T , LRG_482:g.1102589G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.98-27G>T MANE Select ENSP00000501943.1:n.98-27G>T
ENST00000300305.7:c.98-27G>T ENSP00000300305.3:n.98-27G>T
ENST00000344691.8:c.-11G>T ENSP00000340690.4:n.-11G>T
ENST00000358356.9:c.-11G>T ENSP00000351123.5:n.-11G>T
ENST00000399237.6:c.62-27G>T ENSP00000382182.2:n.62-27G>T
ENST00000399240.5:c.-11G>T ENSP00000382184.1:n.-11G>T
ENST00000437180.5:c.98-27G>T ENSP00000409227.1:n.98-27G>T
ENST00000455571.5:c.59-27G>T ENSP00000388189.1:n.59-27G>T
ENST00000475045.6:c.98-27G>T ENSP00000477072.1:n.98-27G>T
ENST00000482318.5:c.59-6410G>T ENSP00000477067.1:n.59-6410G>T
NM_001001890.2:c.-11G>T NP_001001890.1:n.-11G>T
NM_001122607.1:c.-11G>T NP_001116079.1:n.-11G>T
NM_001754.4:c.98-27G>T , LRG_482t1:c.98-27G>T NP_001745.2:n.98-27G>T
XM_005261068.3:c.62-27G>T XP_005261125.1:n.62-27G>T
XM_005261069.3:c.98-27G>T XP_005261126.1:n.98-27G>T
XM_011529766.1:c.98-27G>T XP_011528068.1:n.98-27G>T
XM_011529767.1:c.59-27G>T XP_011528069.1:n.59-27G>T
XM_011529768.1:c.59-27G>T XP_011528070.1:n.59-27G>T
XM_011529770.1:c.98-27G>T XP_011528072.1:n.98-27G>T
XR_937576.1:n.277-27G>T
XM_005261069.4:c.98-27G>T XP_005261126.1:n.98-27G>T
XM_011529766.2:c.98-27G>T XP_011528068.1:n.98-27G>T
XM_011529767.2:c.59-27G>T XP_011528069.1:n.59-27G>T
XM_011529768.2:c.59-27G>T XP_011528070.1:n.59-27G>T
XM_011529770.2:c.98-27G>T XP_011528072.1:n.98-27G>T
XM_017028487.1:c.-56-27G>T XP_016883976.1:n.-56-27G>T
XR_937576.2:n.324-27G>T
NM_001001890.3:c.-11G>T NP_001001890.1:n.-11G>T
NM_001122607.2:c.-11G>T NP_001116079.1:n.-11G>T
NM_001754.5:c.98-27G>T MANE Select NP_001745.2:n.98-27G>T
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