Canonical Allele Identifier: CA2710263406

Gene: CSF1R

Linked Data

• dbSNP Id: rs2113782169

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057419A>C , CM000667.2:g.150057419A>C	GRCh38
NC_000005.9:g.149436982A>C , CM000667.1:g.149436982A>C	GRCh37
NC_000005.8:g.149417175A>C	NCBI36
NG_012303.1:g.60954T>G
NG_012303.2:g.60954T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2222-35T>G MANE Select	ENSP00000501699.1:n.2222-35T>G
ENST00000286301.7:c.2222-35T>G	ENSP00000286301.3:n.2222-35T>G
ENST00000504875.5:c.*43-35T>G	ENSP00000422212.1:n.*43-35T>G
ENST00000515068.1:c.391-35T>G	ENSP00000427545.1:n.391-35T>G
NM_001288705.1:c.2222-35T>G	NP_001275634.1:n.2222-35T>G
NM_005211.3:c.2222-35T>G	NP_005202.2:n.2222-35T>G
NR_109969.1:n.2272-35T>G
NM_001288705.2:c.2222-35T>G	NP_001275634.1:n.2222-35T>G
NM_001349736.1:c.2222-35T>G	NP_001336665.1:n.2222-35T>G
NM_001288705.3:c.2222-35T>G MANE Select	NP_001275634.1:n.2222-35T>G
NM_001375320.1:c.2222-35T>G	NP_001362249.1:n.2222-35T>G
NM_001375321.1:c.1778-35T>G	NP_001362250.1:n.1778-35T>G
NR_164679.1:n.2115-35T>G
NM_001349736.2:c.2222-35T>G	NP_001336665.1:n.2222-35T>G
NM_005211.4:c.2222-35T>G	NP_005202.2:n.2222-35T>G
NR_109969.2:n.2186-35T>G