Canonical Allele Identifier: CA2648792059

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589848-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589849dup , CM000663.2:g.161589849dup	GRCh38
NC_000001.10:g.161559639dup , CM000663.1:g.161559639dup	GRCh37
NC_000001.9:g.159826263dup	NCBI36
NG_011982.1:g.13511dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40818dup	ENSP00000514363.1:n.41-40818dup
ENST00000699403.1:c.61+40519dup	ENSP00000514364.1:n.61+40519dup
ENST00000465075.6:n.483+30dup
ENST00000466542.6:c.391+30dup	ENSP00000426627.1:n.391+30dup
ENST00000473530.6:n.572+30dup
ENST00000473712.6:n.413+30dup
ENST00000482226.2:n.370+30dup
ENST00000496692.6:n.517dup
ENST00000543859.5:c.388+30dup	ENSP00000444663.2:n.388+30dup
ENST00000611236.1:c.388+30dup	ENSP00000480953.1:n.388+30dup
NR_047648.1:n.490+30dup