Canonical Allele Identifier: CA563956084

Gene: CSF1R

Linked Data

• dbSNP Id: rs1371291378
• gnomAD v2: 5-149449968-C-T
• gnomAD v3: 5-150070405-C-T
• gnomAD v4: 5-150070405-C-T
• MyVariant Identifiers: chr5:g.149449968C>T (hg19) ; chr5:g.150070405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150070405C>T , CM000667.2:g.150070405C>T	GRCh38
NC_000005.9:g.149449968C>T , CM000667.1:g.149449968C>T	GRCh37
NC_000005.8:g.149430161C>T	NCBI36
NG_012303.1:g.47968G>A
NG_012303.2:g.47968G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1198+51G>A MANE Select	ENSP00000501699.1:n.1198+51G>A
ENST00000286301.7:c.1198+51G>A	ENSP00000286301.3:n.1198+51G>A
ENST00000504875.5:c.1198+51G>A	ENSP00000422212.1:n.1198+51G>A
NM_001288705.1:c.1198+51G>A	NP_001275634.1:n.1198+51G>A
NM_005211.3:c.1198+51G>A	NP_005202.2:n.1198+51G>A
NR_109969.1:n.1411+51G>A
NM_001288705.2:c.1198+51G>A	NP_001275634.1:n.1198+51G>A
NM_001349736.1:c.1198+51G>A	NP_001336665.1:n.1198+51G>A
NM_001288705.3:c.1198+51G>A MANE Select	NP_001275634.1:n.1198+51G>A
NM_001375320.1:c.1198+51G>A	NP_001362249.1:n.1198+51G>A
NM_001375321.1:c.754+51G>A	NP_001362250.1:n.754+51G>A
NR_164679.1:n.1254+51G>A
NM_001349736.2:c.1198+51G>A	NP_001336665.1:n.1198+51G>A
NM_005211.4:c.1198+51G>A	NP_005202.2:n.1198+51G>A
NR_109969.2:n.1325+51G>A