Canonical Allele Identifier: CA748986410
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1342202275
gnomAD v3: 21-35641378-G-T
gnomAD v4: 21-35641378-G-T
MyVariant Identifiers: chr21:g.37013676G>T (hg19) chr21:g.35641378G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641378G>T , CM000683.2:g.35641378G>T GRCh38
NC_000021.8:g.37013676G>T , CM000683.1:g.37013676G>T GRCh37
NC_000021.7:g.35935546G>T NCBI36
NG_011402.2:g.348333C>A , LRG_482:g.348333C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13442C>A ENSP00000477072.1:n.-532+13442C>A
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