Canonical Allele Identifier: CA320423789
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs191931405
gnomAD v3: 21-35641349-T-A
gnomAD v4: 21-35641349-T-A
MyVariant Identifiers: chr21:g.37013647T>A (hg19) chr21:g.35641349T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641349T>A , CM000683.2:g.35641349T>A GRCh38
NC_000021.8:g.37013647T>A , CM000683.1:g.37013647T>A GRCh37
NC_000021.7:g.35935517T>A NCBI36
NG_011402.2:g.348362A>T , LRG_482:g.348362A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13471A>T ENSP00000477072.1:n.-532+13471A>T
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