Canonical Allele Identifier: CA31680405

Gene: FCGR2C

Linked Data

• dbSNP Id: rs776682989
• gnomAD v2: 1-161559432-CG-C
• gnomAD v4: 1-161589642-CG-C
• MyVariant Identifiers: chr1:g.161559433del (hg19) ; chr1:g.161589643del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589647del , CM000663.2:g.161589647del	GRCh38
NC_000001.10:g.161559437del , CM000663.1:g.161559437del	GRCh37
NC_000001.9:g.159826061del	NCBI36
NG_011982.1:g.13309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40612del	ENSP00000514363.1:n.41-40612del
ENST00000699403.1:c.61+40725del	ENSP00000514364.1:n.61+40725del
ENST00000465075.6:n.311del
ENST00000466542.6:c.219del	ENSP00000426627.1:p.Thr74LeufsTer?
ENST00000473530.6:n.400del
ENST00000473712.6:n.241del
ENST00000482226.2:n.198del
ENST00000496692.6:n.315del
ENST00000502411.5:n.516del
ENST00000543859.5:c.216del	ENSP00000444663.2:p.Thr73LeufsTer?
ENST00000611236.1:c.216del	ENSP00000480953.1:p.Thr73LeufsTer?
NR_047648.1:n.318del