Canonical Allele Identifier: CA410205752
Gene: RUNX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.36265249C>G (hg19) chr21:g.34892952C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34892952C>G , CM000683.2:g.34892952C>G GRCh38
NC_000021.8:g.36265249C>G , CM000683.1:g.36265249C>G GRCh37
NC_000021.7:g.35187119C>G NCBI36
NG_011402.2:g.1096760G>C , LRG_482:g.1096760G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.70G>C MANE Select ENSP00000501943.1:p.Gly24Arg
ENST00000300305.7:c.70G>C ENSP00000300305.3:p.Gly24Arg
ENST00000416754.1:c.70G>C ENSP00000405158.1:p.Gly24Arg
ENST00000437180.5:c.70G>C ENSP00000409227.1:p.Gly24Arg
ENST00000455571.5:c.59-5856G>C ENSP00000388189.1:n.59-5856G>C
ENST00000475045.6:c.70G>C ENSP00000477072.1:p.Gly24Arg
ENST00000482318.5:c.59-12239G>C ENSP00000477067.1:n.59-12239G>C
NM_001754.4:c.70G>C , LRG_482t1:c.70G>C NP_001745.2:p.Gly24Arg
XM_005261069.3:c.70G>C XP_005261126.1:p.Gly24Arg
XM_011529766.1:c.70G>C XP_011528068.1:p.Gly24Arg
XM_011529767.1:c.59-5856G>C XP_011528069.1:n.59-5856G>C
XM_011529768.1:c.59-5856G>C XP_011528070.1:n.59-5856G>C
XM_011529770.1:c.70G>C XP_011528072.1:p.Gly24Arg
XR_937576.1:n.249G>C
XM_005261069.4:c.70G>C XP_005261126.1:p.Gly24Arg
XM_011529766.2:c.70G>C XP_011528068.1:p.Gly24Arg
XM_011529767.2:c.59-5856G>C XP_011528069.1:n.59-5856G>C
XM_011529768.2:c.59-5856G>C XP_011528070.1:n.59-5856G>C
XM_011529770.2:c.70G>C XP_011528072.1:p.Gly24Arg
XR_937576.2:n.296G>C
NM_001754.5:c.70G>C MANE Select NP_001745.2:p.Gly24Arg
Search 100 bp 5'
Search 100 bp 3'