Canonical Allele Identifier: CA320423786
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs762008683
gnomAD v3: 21-35641342-T-G
gnomAD v4: 21-35641342-T-G
MyVariant Identifiers: chr21:g.37013640T>G (hg19) chr21:g.35641342T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641342T>G , CM000683.2:g.35641342T>G GRCh38
NC_000021.8:g.37013640T>G , CM000683.1:g.37013640T>G GRCh37
NC_000021.7:g.35935510T>G NCBI36
NG_011402.2:g.348369A>C , LRG_482:g.348369A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13478A>C ENSP00000477072.1:n.-532+13478A>C
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