Canonical Allele Identifier: CA2648792083

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589933-G-GAGGCAACTCACAGCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589933_161589934insAGGCAACTCACAGCGA , CM000663.2:g.161589933_161589934insAGGCAACTCACAGCGA	GRCh38
NC_000001.10:g.161559723_161559724insAGGCAACTCACAGCGA , CM000663.1:g.161559723_161559724insAGGCAACTCACAGCGA	GRCh37
NC_000001.9:g.159826347_159826348insAGGCAACTCACAGCGA	NCBI36
NG_011982.1:g.13595_13596insAGGCAACTCACAGCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40903_41-40902insTCGCTGTGAGTTGCCT	ENSP00000514363.1:n.41-40903_41-40902insTCGCTGTGAGTTGCCT
ENST00000699403.1:c.61+40434_61+40435insTCGCTGTGAGTTGCCT	ENSP00000514364.1:n.61+40434_61+40435insTCGCTGTGAGTTGCCT
ENST00000465075.6:n.483+114_483+115insAGGCAACTCACAGCGA
ENST00000466542.6:c.391+114_391+115insAGGCAACTCACAGCGA	ENSP00000426627.1:n.391+114_391+115insAGGCAACTCACAGCGA
ENST00000473530.6:n.572+114_572+115insAGGCAACTCACAGCGA
ENST00000473712.6:n.413+114_413+115insAGGCAACTCACAGCGA
ENST00000482226.2:n.370+114_370+115insAGGCAACTCACAGCGA
ENST00000543859.5:c.388+114_388+115insAGGCAACTCACAGCGA	ENSP00000444663.2:n.388+114_388+115insAGGCAACTCACAGCGA
ENST00000611236.1:c.388+114_388+115insAGGCAACTCACAGCGA	ENSP00000480953.1:n.388+114_388+115insAGGCAACTCACAGCGA
NR_047648.1:n.490+114_490+115insAGGCAACTCACAGCGA