Canonical Allele Identifier: CA527135548

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1164115176
• gnomAD v2: 1-161559547-A-ATCCC
• MyVariant Identifiers: chr1:g.161559547_161559548insTCCC (hg19) ; chr1:g.161589757_161589758insTCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589757_161589758insTCCC , CM000663.2:g.161589757_161589758insTCCC	GRCh38
NC_000001.10:g.161559547_161559548insTCCC , CM000663.1:g.161559547_161559548insTCCC	GRCh37
NC_000001.9:g.159826171_159826172insTCCC	NCBI36
NG_011982.1:g.13419_13420insTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40727_41-40726insGGGA	ENSP00000514363.1:n.41-40727_41-40726insGGGA
ENST00000699403.1:c.61+40610_61+40611insGGGA	ENSP00000514364.1:n.61+40610_61+40611insGGGA
ENST00000465075.6:n.421_422insTCCC
ENST00000466542.6:c.329_330insTCCC	ENSP00000426627.1:p.Glu110AspfsTer23
ENST00000473530.6:n.510_511insTCCC
ENST00000473712.6:n.351_352insTCCC
ENST00000482226.2:n.308_309insTCCC
ENST00000496692.6:n.425_426insTCCC
ENST00000543859.5:c.326_327insTCCC	ENSP00000444663.2:p.Glu109AspfsTer23
ENST00000611236.1:c.326_327insTCCC	ENSP00000480953.1:p.Glu109AspfsTer23
NR_047648.1:n.428_429insTCCC