Canonical Allele Identifier: CA1202800875

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589990_161589992delinsGAA , CM000663.2:g.161589990_161589992delinsGAA	GRCh38
NC_000001.10:g.161559780_161559782delinsGAA , CM000663.1:g.161559780_161559782delinsGAA	GRCh37
NC_000001.9:g.159826404_159826406delinsGAA	NCBI36
NG_011982.1:g.13652_13654delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40961_41-40959delinsTTC	ENSP00000514363.1:n.41-40961_41-40959delinsTTC
ENST00000699403.1:c.61+40376_61+40378delinsTTC	ENSP00000514364.1:n.61+40376_61+40378delinsTTC
ENST00000465075.6:n.484-91_484-89delinsGAA
ENST00000466542.6:c.391+171_391+173delinsGAA	ENSP00000426627.1:n.391+171_391+173delinsGAA
ENST00000473530.6:n.572+171_572+173delinsGAA
ENST00000473712.6:n.413+171_413+173delinsGAA
ENST00000482226.2:n.370+171_370+173delinsGAA
ENST00000543859.5:c.388+171_388+173delinsGAA	ENSP00000444663.2:n.388+171_388+173delinsGAA
ENST00000611236.1:c.388+171_388+173delinsGAA	ENSP00000480953.1:n.388+171_388+173delinsGAA
NR_047648.1:n.490+171_490+173delinsGAA