Canonical Allele Identifier: CA2654375791
Gene: RUNX1 HGNC NCBI

Linked Data

gnomAD v4: 21-34789891-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34789891T>C , CM000683.2:g.34789891T>C GRCh38
NC_000021.8:g.36162188T>C , CM000683.1:g.36162188T>C GRCh37
NC_000021.7:g.35084058T>C NCBI36
NG_011402.2:g.1199821A>G , LRG_482:g.1199821A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.*2244A>G MANE Select ENSP00000501943.1:n.*2244A>G
ENST00000300305.7:c.*2244A>G ENSP00000300305.3:n.*2244A>G
ENST00000344691.8:c.*2244A>G ENSP00000340690.4:n.*2244A>G
ENST00000437180.5:c.*2244A>G ENSP00000409227.1:n.*2244A>G
NM_001001890.2:c.*2244A>G NP_001001890.1:n.*2244A>G
NM_001754.4:c.*2244A>G , LRG_482t1:c.*2244A>G NP_001745.2:n.*2244A>G
XM_005261068.3:c.*2244A>G XP_005261125.1:n.*2244A>G
XM_005261069.3:c.*2244A>G XP_005261126.1:n.*2244A>G
XM_011529766.1:c.*2244A>G XP_011528068.1:n.*2244A>G
XM_011529767.1:c.*2244A>G XP_011528069.1:n.*2244A>G
XM_011529768.1:c.*2244A>G XP_011528070.1:n.*2244A>G
XM_005261069.4:c.*2244A>G XP_005261126.1:n.*2244A>G
XM_011529766.2:c.*2244A>G XP_011528068.1:n.*2244A>G
XM_011529767.2:c.*2244A>G XP_011528069.1:n.*2244A>G
XM_011529768.2:c.*2244A>G XP_011528070.1:n.*2244A>G
XM_017028487.1:c.*2244A>G XP_016883976.1:n.*2244A>G
NM_001001890.3:c.*2244A>G NP_001001890.1:n.*2244A>G
NM_001754.5:c.*2244A>G MANE Select NP_001745.2:n.*2244A>G
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