Canonical Allele Identifier: CA1202800482

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589739A= , CM000663.2:g.161589739A=	GRCh38
NC_000001.10:g.161559529A= , CM000663.1:g.161559529A=	GRCh37
NC_000001.9:g.159826153A=	NCBI36
NG_011982.1:g.13401A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40708T=	ENSP00000514363.1:n.41-40708T=
ENST00000699403.1:c.61+40629T=	ENSP00000514364.1:n.61+40629T=
ENST00000465075.6:n.403A=
ENST00000466542.6:c.311A=	ENSP00000426627.1:p.Asn104=
ENST00000473530.6:n.492A=
ENST00000473712.6:n.333A=
ENST00000482226.2:n.290A=
ENST00000496692.6:n.407A=
ENST00000543859.5:c.308A=	ENSP00000444663.2:p.Asn103=
ENST00000611236.1:c.308A=	ENSP00000480953.1:p.Asn103=
NR_047648.1:n.410A=