Canonical Allele Identifier: CA11947665
Gene: CSF1R HGNC NCBI

Linked Data

dbSNP Id: rs1549919

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150073887T>C , CM000667.2:g.150073887T>C GRCh38
NC_000005.9:g.149453450T>C , CM000667.1:g.149453450T>C GRCh37
NC_000005.8:g.149433643T>C NCBI36
NG_012303.1:g.44486A>G
NG_012303.2:g.44486A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675795.1:c.890-394A>G MANE Select ENSP00000501699.1:n.890-394A>G
ENST00000286301.7:c.890-394A>G ENSP00000286301.3:n.890-394A>G
ENST00000504875.5:c.890-394A>G ENSP00000422212.1:n.890-394A>G
ENST00000543093.1:c.890-3316A>G ENSP00000445282.1:n.890-3316A>G
NM_001288705.1:c.890-394A>G NP_001275634.1:n.890-394A>G
NM_005211.3:c.890-394A>G NP_005202.2:n.890-394A>G
NR_109969.1:n.1103-394A>G
NM_001288705.2:c.890-394A>G NP_001275634.1:n.890-394A>G
NM_001349736.1:c.890-394A>G NP_001336665.1:n.890-394A>G
NM_001288705.3:c.890-394A>G MANE Select NP_001275634.1:n.890-394A>G
NM_001375320.1:c.890-394A>G NP_001362249.1:n.890-394A>G
NM_001375321.1:c.446-394A>G NP_001362250.1:n.446-394A>G
NR_164679.1:n.946-394A>G
NM_001349736.2:c.890-394A>G NP_001336665.1:n.890-394A>G
NM_005211.4:c.890-394A>G NP_005202.2:n.890-394A>G
NR_109969.2:n.1017-394A>G