Canonical Allele Identifier: CA2387638562
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.35641390A= , CM000683.2:g.35641390A= GRCh38
NC_000021.8:g.37013688A= , CM000683.1:g.37013688A= GRCh37
NC_000021.7:g.35935558A= NCBI36
NG_011402.2:g.348321T= , LRG_482:g.348321T=

Transcript Alleles

HGVS Amino-acid change
ENST00000475045.6:c.-532+13430T= ENSP00000477072.1:n.-532+13430T=