Canonical Allele Identifier: CA2648792156

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589994-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589995_161589996del , CM000663.2:g.161589995_161589996del	GRCh38
NC_000001.10:g.161559785_161559786del , CM000663.1:g.161559785_161559786del	GRCh37
NC_000001.9:g.159826409_159826410del	NCBI36
NG_011982.1:g.13657_13658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40965_41-40964del	ENSP00000514363.1:n.41-40965_41-40964del
ENST00000699403.1:c.61+40372_61+40373del	ENSP00000514364.1:n.61+40372_61+40373del
ENST00000465075.6:n.484-86_484-85del
ENST00000466542.6:c.391+176_391+177del	ENSP00000426627.1:n.391+176_391+177del
ENST00000473530.6:n.572+176_572+177del
ENST00000473712.6:n.413+176_413+177del
ENST00000482226.2:n.370+176_370+177del
ENST00000543859.5:c.388+176_388+177del	ENSP00000444663.2:n.388+176_388+177del
ENST00000611236.1:c.388+176_388+177del	ENSP00000480953.1:n.388+176_388+177del
NR_047648.1:n.490+176_490+177del