Canonical Allele Identifier: CA1202800498

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589748A= , CM000663.2:g.161589748A=	GRCh38
NC_000001.10:g.161559538A= , CM000663.1:g.161559538A=	GRCh37
NC_000001.9:g.159826162A=	NCBI36
NG_011982.1:g.13410A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40717T=	ENSP00000514363.1:n.41-40717T=
ENST00000699403.1:c.61+40620T=	ENSP00000514364.1:n.61+40620T=
ENST00000465075.6:n.412A=
ENST00000466542.6:c.320A=	ENSP00000426627.1:p.Asp107=
ENST00000473530.6:n.501A=
ENST00000473712.6:n.342A=
ENST00000482226.2:n.299A=
ENST00000496692.6:n.416A=
ENST00000543859.5:c.317A=	ENSP00000444663.2:p.Asp106=
ENST00000611236.1:c.317A=	ENSP00000480953.1:p.Asp106=
NR_047648.1:n.419A=