Canonical Allele Identifier: CA2648792051

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589605-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589607dup , CM000663.2:g.161589607dup	GRCh38
NC_000001.10:g.161559397dup , CM000663.1:g.161559397dup	GRCh37
NC_000001.9:g.159826021dup	NCBI36
NG_011982.1:g.13269dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40575dup	ENSP00000514363.1:n.41-40575dup
ENST00000699403.1:c.61+40762dup	ENSP00000514364.1:n.61+40762dup
ENST00000465075.6:n.271dup
ENST00000466542.6:c.179dup	ENSP00000426627.1:p.Asn60LysfsTer19
ENST00000473530.6:n.360dup
ENST00000473712.6:n.201dup
ENST00000482226.2:n.158dup
ENST00000496692.6:n.275dup
ENST00000502411.5:n.476dup
ENST00000543859.5:c.176dup	ENSP00000444663.2:p.Asn59LysfsTer19
ENST00000611236.1:c.176dup	ENSP00000480953.1:p.Asn59LysfsTer19
NR_047648.1:n.278dup