Canonical Allele Identifier: CA3506502
Gene: CSF1R HGNC NCBI

Linked Data

dbSNP Id: rs764658321

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150057409C>A , CM000667.2:g.150057409C>A GRCh38
NC_000005.9:g.149436972C>A , CM000667.1:g.149436972C>A GRCh37
NC_000005.8:g.149417165C>A NCBI36
NG_012303.1:g.60964G>T
NG_012303.2:g.60964G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.2222-25G>T MANE Select ENSP00000501699.1:n.2222-25G>T
ENST00000286301.7:c.2222-25G>T ENSP00000286301.3:n.2222-25G>T
ENST00000504875.5:c.*43-25G>T ENSP00000422212.1:n.*43-25G>T
ENST00000515068.1:c.391-25G>T ENSP00000427545.1:n.391-25G>T
NM_001288705.1:c.2222-25G>T NP_001275634.1:n.2222-25G>T
NM_005211.3:c.2222-25G>T NP_005202.2:n.2222-25G>T
NR_109969.1:n.2272-25G>T
NM_001288705.2:c.2222-25G>T NP_001275634.1:n.2222-25G>T
NM_001349736.1:c.2222-25G>T NP_001336665.1:n.2222-25G>T
NM_001288705.3:c.2222-25G>T MANE Select NP_001275634.1:n.2222-25G>T
NM_001375320.1:c.2222-25G>T NP_001362249.1:n.2222-25G>T
NM_001375321.1:c.1778-25G>T NP_001362250.1:n.1778-25G>T
NR_164679.1:n.2115-25G>T
NM_001349736.2:c.2222-25G>T NP_001336665.1:n.2222-25G>T
NM_005211.4:c.2222-25G>T NP_005202.2:n.2222-25G>T
NR_109969.2:n.2186-25G>T