Canonical Allele Identifier: CA890206310

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1412993278
• gnomAD v4: 1-161589985-CAGA-C
• MyVariant Identifiers: chr1:g.161559776_161559778del (hg19) ; chr1:g.161589986_161589988del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589992_161589994del , CM000663.2:g.161589992_161589994del	GRCh38
NC_000001.10:g.161559782_161559784del , CM000663.1:g.161559782_161559784del	GRCh37
NC_000001.9:g.159826406_159826408del	NCBI36
NG_011982.1:g.13654_13656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40957_41-40955del	ENSP00000514363.1:n.41-40957_41-40955del
ENST00000699403.1:c.61+40380_61+40382del	ENSP00000514364.1:n.61+40380_61+40382del
ENST00000465075.6:n.484-89_484-87del
ENST00000466542.6:c.391+173_391+175del	ENSP00000426627.1:n.391+173_391+175del
ENST00000473530.6:n.572+173_572+175del
ENST00000473712.6:n.413+173_413+175del
ENST00000482226.2:n.370+173_370+175del
ENST00000543859.5:c.388+173_388+175del	ENSP00000444663.2:n.388+173_388+175del
ENST00000611236.1:c.388+173_388+175del	ENSP00000480953.1:n.388+173_388+175del
NR_047648.1:n.490+173_490+175del