Canonical Allele Identifier: CA320178446
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs111564619
MyVariant Identifiers: chr21:g.36673506A>T (hg19) chr21:g.35301208A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35301208A>T , CM000683.2:g.35301208A>T GRCh38
NC_000021.8:g.36673506A>T , CM000683.1:g.36673506A>T GRCh37
NC_000021.7:g.35595376A>T NCBI36
NG_011402.2:g.688503T>A , LRG_482:g.688503T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-197+160753T>A ENSP00000477072.1:n.-197+160753T>A
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