Canonical Allele Identifier: CA129070413

Gene: CSF1R

Linked Data

• dbSNP Id: rs963826838
• gnomAD v4: 5-150073160-G-T
• MyVariant Identifiers: chr5:g.149452723G>T (hg19) ; chr5:g.150073160G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150073160G>T , CM000667.2:g.150073160G>T	GRCh38
NC_000005.9:g.149452723G>T , CM000667.1:g.149452723G>T	GRCh37
NC_000005.8:g.149432916G>T	NCBI36
NG_012303.1:g.45213C>A
NG_012303.2:g.45213C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.1082+141C>A MANE Select	ENSP00000501699.1:n.1082+141C>A
ENST00000286301.7:c.1082+141C>A	ENSP00000286301.3:n.1082+141C>A
ENST00000504875.5:c.1082+141C>A	ENSP00000422212.1:n.1082+141C>A
ENST00000543093.1:c.890-2589C>A	ENSP00000445282.1:n.890-2589C>A
NM_001288705.1:c.1082+141C>A	NP_001275634.1:n.1082+141C>A
NM_005211.3:c.1082+141C>A	NP_005202.2:n.1082+141C>A
NR_109969.1:n.1295+141C>A
NM_001288705.2:c.1082+141C>A	NP_001275634.1:n.1082+141C>A
NM_001349736.1:c.1082+141C>A	NP_001336665.1:n.1082+141C>A
NM_001288705.3:c.1082+141C>A MANE Select	NP_001275634.1:n.1082+141C>A
NM_001375320.1:c.1082+141C>A	NP_001362249.1:n.1082+141C>A
NM_001375321.1:c.638+141C>A	NP_001362250.1:n.638+141C>A
NR_164679.1:n.1138+141C>A
NM_001349736.2:c.1082+141C>A	NP_001336665.1:n.1082+141C>A
NM_005211.4:c.1082+141C>A	NP_005202.2:n.1082+141C>A
NR_109969.2:n.1209+141C>A