Canonical Allele Identifier: CA2770895578
Gene: RUNX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45390311T>C , CM000668.2:g.45390311T>C GRCh38
NC_000006.11:g.45358048T>C , CM000668.1:g.45358048T>C GRCh37
NC_000006.10:g.45466026T>C NCBI36
NG_008020.1:g.66995T>C
NG_008020.2:g.66995T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647337.2:c.59-32282T>C MANE Select ENSP00000495497.1:n.59-32282T>C
ENST00000371432.7:c.59-32282T>C ENSP00000360486.4:n.59-32282T>C
ENST00000371436.10:c.59-32282T>C ENSP00000360491.6:n.59-32282T>C
ENST00000371438.5:c.59-32282T>C ENSP00000360493.1:n.59-32282T>C
ENST00000465038.6:c.59-32282T>C ENSP00000420707.2:n.59-32282T>C
ENST00000483377.5:c.59-41552T>C ENSP00000461357.1:n.59-41552T>C
ENST00000576263.5:c.59-32282T>C ENSP00000458178.1:n.59-32282T>C
NM_001015051.3:c.59-32282T>C NP_001015051.3:n.59-32282T>C
NM_001024630.3:c.59-32282T>C NP_001019801.3:n.59-32282T>C
XM_011514960.1:c.263-32282T>C XP_011513262.1:n.263-32282T>C
XM_011514961.1:c.263-32282T>C XP_011513263.1:n.263-32282T>C
XM_011514962.1:c.263-32282T>C XP_011513264.1:n.263-32282T>C
XM_011514963.1:c.263-32282T>C XP_011513265.1:n.263-32282T>C
XM_011514964.1:c.263-32282T>C XP_011513266.1:n.263-32282T>C
XM_011514965.1:c.263-32282T>C XP_011513267.1:n.263-32282T>C
XM_011514967.1:c.263-32282T>C XP_011513269.1:n.263-32282T>C
XM_011514968.1:c.263-32282T>C XP_011513270.1:n.263-32282T>C
XR_926323.1:n.775-32282T>C
NM_001024630.4:c.59-32282T>C MANE Select NP_001019801.3:n.59-32282T>C
NM_001015051.4:c.59-32282T>C NP_001015051.3:n.59-32282T>C