Canonical Allele Identifier: CA748969260
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1326760997
gnomAD v3: 21-35301224-C-A
gnomAD v4: 21-35301224-C-A
MyVariant Identifiers: chr21:g.36673522C>A (hg19) chr21:g.35301224C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35301224C>A , CM000683.2:g.35301224C>A GRCh38
NC_000021.8:g.36673522C>A , CM000683.1:g.36673522C>A GRCh37
NC_000021.7:g.35595392C>A NCBI36
NG_011402.2:g.688487G>T , LRG_482:g.688487G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-197+160737G>T ENSP00000477072.1:n.-197+160737G>T
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