Canonical Allele Identifier: CA748986404
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1269269653
gnomAD v3: 21-35641353-T-G
gnomAD v4: 21-35641353-T-G
MyVariant Identifiers: chr21:g.37013651T>G (hg19) chr21:g.35641353T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641353T>G , CM000683.2:g.35641353T>G GRCh38
NC_000021.8:g.37013651T>G , CM000683.1:g.37013651T>G GRCh37
NC_000021.7:g.35935521T>G NCBI36
NG_011402.2:g.348358A>C , LRG_482:g.348358A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13467A>C ENSP00000477072.1:n.-532+13467A>C
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