Canonical Allele Identifier: CA3506989
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1415854
dbSNP Id: rs747597752

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073459G>C , CM000667.2:g.150073459G>C GRCh38
NC_000005.9:g.149453022G>C , CM000667.1:g.149453022G>C GRCh37
NC_000005.8:g.149433215G>C NCBI36
NG_012303.1:g.44914C>G
NG_012303.2:g.44914C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.924C>G MANE Select ENSP00000501699.1:p.Asn308Lys
ENST00000286301.7:c.924C>G ENSP00000286301.3:p.Asn308Lys
ENST00000504875.5:c.924C>G ENSP00000422212.1:p.Asn308Lys
ENST00000543093.1:c.890-2888C>G ENSP00000445282.1:n.890-2888C>G
NM_001288705.1:c.924C>G NP_001275634.1:p.Asn308Lys
NM_005211.3:c.924C>G NP_005202.2:p.Asn308Lys
NR_109969.1:n.1137C>G
NM_001288705.2:c.924C>G NP_001275634.1:p.Asn308Lys
NM_001349736.1:c.924C>G NP_001336665.1:p.Asn308Lys
NM_001288705.3:c.924C>G MANE Select NP_001275634.1:p.Asn308Lys
NM_001375320.1:c.924C>G NP_001362249.1:p.Asn308Lys
NM_001375321.1:c.480C>G NP_001362250.1:p.Asn160Lys
NR_164679.1:n.980C>G
NM_001349736.2:c.924C>G NP_001336665.1:p.Asn308Lys
NM_005211.4:c.924C>G NP_005202.2:p.Asn308Lys
NR_109969.2:n.1051C>G