Canonical Allele Identifier: CA748969246
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1267163118
MyVariant Identifiers: chr21:g.36673492G>A (hg19) chr21:g.35301194G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35301194G>A , CM000683.2:g.35301194G>A GRCh38
NC_000021.8:g.36673492G>A , CM000683.1:g.36673492G>A GRCh37
NC_000021.7:g.35595362G>A NCBI36
NG_011402.2:g.688517C>T , LRG_482:g.688517C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-197+160767C>T ENSP00000477072.1:n.-197+160767C>T
Search 100 bp 5'
Search 100 bp 3'