Canonical Allele Identifier: CA1022101988
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1982582571

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641343G>A , CM000683.2:g.35641343G>A GRCh38
NC_000021.8:g.37013641G>A , CM000683.1:g.37013641G>A GRCh37
NC_000021.7:g.35935511G>A NCBI36
NG_011402.2:g.348368C>T , LRG_482:g.348368C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13477C>T ENSP00000477072.1:n.-532+13477C>T