Canonical Allele Identifier: CA3506978
Gene: CSF1R HGNC NCBI

Linked Data

dbSNP Id: rs759387562

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073423G>A , CM000667.2:g.150073423G>A GRCh38
NC_000005.9:g.149452986G>A , CM000667.1:g.149452986G>A GRCh37
NC_000005.8:g.149433179G>A NCBI36
NG_012303.1:g.44950C>T
NG_012303.2:g.44950C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.960C>T MANE Select ENSP00000501699.1:p.Asn320=
ENST00000286301.7:c.960C>T ENSP00000286301.3:p.Asn320=
ENST00000504875.5:c.960C>T ENSP00000422212.1:p.Asn320=
ENST00000543093.1:c.890-2852C>T ENSP00000445282.1:n.890-2852C>T
NM_001288705.1:c.960C>T NP_001275634.1:p.Asn320=
NM_005211.3:c.960C>T NP_005202.2:p.Asn320=
NR_109969.1:n.1173C>T
NM_001288705.2:c.960C>T NP_001275634.1:p.Asn320=
NM_001349736.1:c.960C>T NP_001336665.1:p.Asn320=
NM_001288705.3:c.960C>T MANE Select NP_001275634.1:p.Asn320=
NM_001375320.1:c.960C>T NP_001362249.1:p.Asn320=
NM_001375321.1:c.516C>T NP_001362250.1:p.Asn172=
NR_164679.1:n.1016C>T
NM_001349736.2:c.960C>T NP_001336665.1:p.Asn320=
NM_005211.4:c.960C>T NP_005202.2:p.Asn320=
NR_109969.2:n.1087C>T