Canonical Allele Identifier: CA1202800356

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589623C= , CM000663.2:g.161589623C=	GRCh38
NC_000001.10:g.161559413C= , CM000663.1:g.161559413C=	GRCh37
NC_000001.9:g.159826037C=	NCBI36
NG_011982.1:g.13285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40592G=	ENSP00000514363.1:n.41-40592G=
ENST00000699403.1:c.61+40745G=	ENSP00000514364.1:n.61+40745G=
ENST00000465075.6:n.287C=
ENST00000466542.6:c.195C=	ENSP00000426627.1:p.Asp65=
ENST00000473530.6:n.376C=
ENST00000473712.6:n.217C=
ENST00000482226.2:n.174C=
ENST00000496692.6:n.291C=
ENST00000502411.5:n.492C=
ENST00000543859.5:c.192C=	ENSP00000444663.2:p.Asp64=
ENST00000611236.1:c.192C=	ENSP00000480953.1:p.Asp64=
NR_047648.1:n.294C=