Canonical Allele Identifier: CA1202800360

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589625C= , CM000663.2:g.161589625C=	GRCh38
NC_000001.10:g.161559415C= , CM000663.1:g.161559415C=	GRCh37
NC_000001.9:g.159826039C=	NCBI36
NG_011982.1:g.13287C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40594G=	ENSP00000514363.1:n.41-40594G=
ENST00000699403.1:c.61+40743G=	ENSP00000514364.1:n.61+40743G=
ENST00000465075.6:n.289C=
ENST00000466542.6:c.197C=	ENSP00000426627.1:p.Ser66=
ENST00000473530.6:n.378C=
ENST00000473712.6:n.219C=
ENST00000482226.2:n.176C=
ENST00000496692.6:n.293C=
ENST00000502411.5:n.494C=
ENST00000543859.5:c.194C=	ENSP00000444663.2:p.Ser65=
ENST00000611236.1:c.194C=	ENSP00000480953.1:p.Ser65=
NR_047648.1:n.296C=