Canonical Allele Identifier: CA1202800621

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589798G= , CM000663.2:g.161589798G=	GRCh38
NC_000001.10:g.161559588G= , CM000663.1:g.161559588G=	GRCh37
NC_000001.9:g.159826212G=	NCBI36
NG_011982.1:g.13460G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40767C=	ENSP00000514363.1:n.41-40767C=
ENST00000699403.1:c.61+40570C=	ENSP00000514364.1:n.61+40570C=
ENST00000465075.6:n.462G=
ENST00000466542.6:c.370G=	ENSP00000426627.1:p.Val124=
ENST00000473530.6:n.551G=
ENST00000473712.6:n.392G=
ENST00000482226.2:n.349G=
ENST00000496692.6:n.466G=
ENST00000543859.5:c.367G=	ENSP00000444663.2:p.Val123=
ENST00000611236.1:c.367G=	ENSP00000480953.1:p.Val123=
NR_047648.1:n.469G=