Canonical Allele Identifier: CA138428363
Gene: RUNX2 HGNC NCBI

Linked Data

dbSNP Id: rs10498760

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45396059C>A , CM000668.2:g.45396059C>A GRCh38
NC_000006.11:g.45363796C>A , CM000668.1:g.45363796C>A GRCh37
NC_000006.10:g.45471774C>A NCBI36
NG_008020.1:g.72743C>A
NG_008020.2:g.72743C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371432.7:c.59-26534C>A ENSP00000360486.4:p.=
ENST00000371436.10:n.59-26534C>A ENSP00000360491.6:p.=
ENST00000371438.5:c.59-26534C>A ENSP00000360493.1:p.=
ENST00000465038.6:c.59-26534C>A ENSP00000420707.2:p.=
ENST00000483377.5:c.59-35804C>A ENSP00000461357.1:p.=
ENST00000576263.5:n.59-26534C>A ENSP00000458178.1:p.=
NM_001015051.3:c.59-26534C>A NP_001015051.3:p.=
NM_001024630.3:c.59-26534C>A NP_001019801.3:p.=
XM_011514960.1:c.263-26534C>A XP_011513262.1:p.=
XM_011514961.1:c.263-26534C>A XP_011513263.1:p.=
XM_011514962.1:c.263-26534C>A XP_011513264.1:p.=
XM_011514963.1:c.263-26534C>A XP_011513265.1:p.=
XM_011514964.1:c.263-26534C>A XP_011513266.1:p.=
XM_011514965.1:c.263-26534C>A XP_011513267.1:p.=
XM_011514967.1:c.263-26534C>A XP_011513269.1:p.=
XM_011514968.1:c.263-26534C>A XP_011513270.1:p.=
NM_001024630.4:c.59-26534C>A MANE Select NP_001019801.3:p.=
NM_001015051.4:c.59-26534C>A NP_001015051.3:p.=