Canonical Allele Identifier: CA1202800646

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589815T= , CM000663.2:g.161589815T=	GRCh38
NC_000001.10:g.161559605T= , CM000663.1:g.161559605T=	GRCh37
NC_000001.9:g.159826229T=	NCBI36
NG_011982.1:g.13477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40784A=	ENSP00000514363.1:n.41-40784A=
ENST00000699403.1:c.61+40553A=	ENSP00000514364.1:n.61+40553A=
ENST00000465075.6:n.479T=
ENST00000466542.6:c.387T=	ENSP00000426627.1:p.Leu129=
ENST00000473530.6:n.568T=
ENST00000473712.6:n.409T=
ENST00000482226.2:n.366T=
ENST00000496692.6:n.483T=
ENST00000543859.5:c.384T=	ENSP00000444663.2:p.Leu128=
ENST00000611236.1:c.384T=	ENSP00000480953.1:p.Leu128=
NR_047648.1:n.486T=