Canonical Allele Identifier: CA1008448821

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589929_161589930insACT , CM000663.2:g.161589929_161589930insACT	GRCh38
NC_000001.10:g.161559719_161559720insACT , CM000663.1:g.161559719_161559720insACT	GRCh37
NC_000001.9:g.159826343_159826344insACT	NCBI36
NG_011982.1:g.13591_13592insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40899_41-40898insAGT	ENSP00000514363.1:n.41-40899_41-40898insAGT
ENST00000699403.1:c.61+40438_61+40439insAGT	ENSP00000514364.1:n.61+40438_61+40439insAGT
ENST00000465075.6:n.483+110_483+111insACT
ENST00000466542.6:c.391+110_391+111insACT	ENSP00000426627.1:n.391+110_391+111insACT
ENST00000473530.6:n.572+110_572+111insACT
ENST00000473712.6:n.413+110_413+111insACT
ENST00000482226.2:n.370+110_370+111insACT
ENST00000543859.5:c.388+110_388+111insACT	ENSP00000444663.2:n.388+110_388+111insACT
ENST00000611236.1:c.388+110_388+111insACT	ENSP00000480953.1:n.388+110_388+111insACT
NR_047648.1:n.490+110_490+111insACT