Canonical Allele Identifier: CA748986418
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1302496850
MyVariant Identifiers: chr21:g.37013693T>C (hg19) chr21:g.35641395T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641395T>C , CM000683.2:g.35641395T>C GRCh38
NC_000021.8:g.37013693T>C , CM000683.1:g.37013693T>C GRCh37
NC_000021.7:g.35935563T>C NCBI36
NG_011402.2:g.348316A>G , LRG_482:g.348316A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13425A>G ENSP00000477072.1:n.-532+13425A>G
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