Canonical Allele Identifier: CA1008448915

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678469107
• gnomAD v3: 1-161589990-GAA-G
• gnomAD v4: 1-161589990-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589991_161589992del , CM000663.2:g.161589991_161589992del	GRCh38
NC_000001.10:g.161559781_161559782del , CM000663.1:g.161559781_161559782del	GRCh37
NC_000001.9:g.159826405_159826406del	NCBI36
NG_011982.1:g.13653_13654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40961_41-40960del	ENSP00000514363.1:n.41-40961_41-40960del
ENST00000699403.1:c.61+40376_61+40377del	ENSP00000514364.1:n.61+40376_61+40377del
ENST00000465075.6:n.484-90_484-89del
ENST00000466542.6:c.391+172_391+173del	ENSP00000426627.1:n.391+172_391+173del
ENST00000473530.6:n.572+172_572+173del
ENST00000473712.6:n.413+172_413+173del
ENST00000482226.2:n.370+172_370+173del
ENST00000543859.5:c.388+172_388+173del	ENSP00000444663.2:n.388+172_388+173del
ENST00000611236.1:c.388+172_388+173del	ENSP00000480953.1:n.388+172_388+173del
NR_047648.1:n.490+172_490+173del