Canonical Allele Identifier: CA3506993
Gene: CSF1R HGNC NCBI

Linked Data

dbSNP Id: rs761676784

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073494_150073495del , CM000667.2:g.150073494_150073495del GRCh38
NC_000005.9:g.149453057_149453058del , CM000667.1:g.149453057_149453058del GRCh37
NC_000005.8:g.149433250_149433251del NCBI36
NG_012303.1:g.44882_44883del
NG_012303.2:g.44882_44883del

Transcript Alleles

HGVS Amino-acid change
ENST00000675795.1:c.892_893del
ENST00000286301.7:c.892_893del
ENST00000504875.5:c.892_893del
ENST00000543093.1:c.890-2920_890-2919del ENSP00000445282.1:n.890-2920_890-2919del
NM_001288705.1:c.892_893del
NM_005211.3:c.892_893del
NR_109969.1:n.1105_1106del
NM_001288705.2:c.892_893del
NM_001349736.1:c.892_893del
NM_001288705.3:c.892_893del
NM_001375320.1:c.892_893del
NM_001375321.1:c.448_449del
NR_164679.1:n.948_949del
NM_001349736.2:c.892_893del
NM_005211.4:c.892_893del
NR_109969.2:n.1019_1020del