Canonical Allele Identifier: CA2648792073

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589914-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589916del , CM000663.2:g.161589916del	GRCh38
NC_000001.10:g.161559706del , CM000663.1:g.161559706del	GRCh37
NC_000001.9:g.159826330del	NCBI36
NG_011982.1:g.13578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40884del	ENSP00000514363.1:n.41-40884del
ENST00000699403.1:c.61+40453del	ENSP00000514364.1:n.61+40453del
ENST00000465075.6:n.483+97del
ENST00000466542.6:c.391+97del	ENSP00000426627.1:n.391+97del
ENST00000473530.6:n.572+97del
ENST00000473712.6:n.413+97del
ENST00000482226.2:n.370+97del
ENST00000543859.5:c.388+97del	ENSP00000444663.2:n.388+97del
ENST00000611236.1:c.388+97del	ENSP00000480953.1:n.388+97del
NR_047648.1:n.490+97del