Canonical Allele Identifier: CA1202800637

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589810G= , CM000663.2:g.161589810G=	GRCh38
NC_000001.10:g.161559600G= , CM000663.1:g.161559600G=	GRCh37
NC_000001.9:g.159826224G=	NCBI36
NG_011982.1:g.13472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40779C=	ENSP00000514363.1:n.41-40779C=
ENST00000699403.1:c.61+40558C=	ENSP00000514364.1:n.61+40558C=
ENST00000465075.6:n.474G=
ENST00000466542.6:c.382G=	ENSP00000426627.1:p.Val128=
ENST00000473530.6:n.563G=
ENST00000473712.6:n.404G=
ENST00000482226.2:n.361G=
ENST00000496692.6:n.478G=
ENST00000543859.5:c.379G=	ENSP00000444663.2:p.Val127=
ENST00000611236.1:c.379G=	ENSP00000480953.1:p.Val127=
NR_047648.1:n.481G=