Canonical Allele Identifier: CA527135547

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1557868772
• gnomAD v2: 1-161559543-GGGGA-G
• gnomAD v4: 1-161589753-GGGGA-G
• MyVariant Identifiers: chr1:g.161559544_161559547del (hg19) ; chr1:g.161589754_161589757del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589755_161589758del , CM000663.2:g.161589755_161589758del	GRCh38
NC_000001.10:g.161559545_161559548del , CM000663.1:g.161559545_161559548del	GRCh37
NC_000001.9:g.159826169_159826172del	NCBI36
NG_011982.1:g.13417_13420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40726_41-40723del	ENSP00000514363.1:n.41-40726_41-40723del
ENST00000699403.1:c.61+40611_61+40614del	ENSP00000514364.1:n.61+40611_61+40614del
ENST00000465075.6:n.419_422del
ENST00000466542.6:c.327_330del	ENSP00000426627.1:p.Glu110ThrfsTer16
ENST00000473530.6:n.508_511del
ENST00000473712.6:n.349_352del
ENST00000482226.2:n.306_309del
ENST00000496692.6:n.423_426del
ENST00000543859.5:c.324_327del	ENSP00000444663.2:p.Glu109ThrfsTer16
ENST00000611236.1:c.324_327del	ENSP00000480953.1:p.Glu109ThrfsTer16
NR_047648.1:n.426_429del