Canonical Allele Identifier: CA2387482817
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1601071664

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35301228T>G , CM000683.2:g.35301228T>G GRCh38
NC_000021.8:g.36673526T>G , CM000683.1:g.36673526T>G GRCh37
NC_000021.7:g.35595396T>G NCBI36
NG_011402.2:g.688483A>C , LRG_482:g.688483A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-197+160733A>C ENSP00000477072.1:n.-197+160733A>C