Canonical Allele Identifier: CA1202800795

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589920G= , CM000663.2:g.161589920G=	GRCh38
NC_000001.10:g.161559710G= , CM000663.1:g.161559710G=	GRCh37
NC_000001.9:g.159826334G=	NCBI36
NG_011982.1:g.13582G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40889C=	ENSP00000514363.1:n.41-40889C=
ENST00000699403.1:c.61+40448C=	ENSP00000514364.1:n.61+40448C=
ENST00000465075.6:n.483+101G=
ENST00000466542.6:c.391+101G=	ENSP00000426627.1:n.391+101G=
ENST00000473530.6:n.572+101G=
ENST00000473712.6:n.413+101G=
ENST00000482226.2:n.370+101G=
ENST00000543859.5:c.388+101G=	ENSP00000444663.2:n.388+101G=
ENST00000611236.1:c.388+101G=	ENSP00000480953.1:n.388+101G=
NR_047648.1:n.490+101G=