Canonical Allele Identifier: CA361760276
Gene: CSF1R HGNC NCBI

Linked Data

dbSNP Id: rs1270799934

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150057369T>C , CM000667.2:g.150057369T>C GRCh38
NC_000005.9:g.149436932T>C , CM000667.1:g.149436932T>C GRCh37
NC_000005.8:g.149417125T>C NCBI36
NG_012303.1:g.61004A>G
NG_012303.2:g.61004A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.2237A>G MANE Select ENSP00000501699.1:p.Asp746Gly
ENST00000286301.7:c.2237A>G ENSP00000286301.3:p.Asp746Gly
ENST00000504875.5:c.*58A>G ENSP00000422212.1:n.*58A>G
ENST00000515068.1:c.406A>G ENSP00000427545.1:n.406A>G
NM_001288705.1:c.2237A>G NP_001275634.1:p.Asp746Gly
NM_005211.3:c.2237A>G NP_005202.2:p.Asp746Gly
NR_109969.1:n.2287A>G
NM_001288705.2:c.2237A>G NP_001275634.1:p.Asp746Gly
NM_001349736.1:c.2237A>G NP_001336665.1:p.Asp746Gly
NM_001288705.3:c.2237A>G MANE Select NP_001275634.1:p.Asp746Gly
NM_001375320.1:c.2237A>G NP_001362249.1:p.Asp746Gly
NM_001375321.1:c.1793A>G NP_001362250.1:p.Asp598Gly
NR_164679.1:n.2130A>G
NM_001349736.2:c.2237A>G NP_001336665.1:p.Asp746Gly
NM_005211.4:c.2237A>G NP_005202.2:p.Asp746Gly
NR_109969.2:n.2201A>G