Canonical Allele Identifier: CA1202800626

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589802A= , CM000663.2:g.161589802A=	GRCh38
NC_000001.10:g.161559592A= , CM000663.1:g.161559592A=	GRCh37
NC_000001.9:g.159826216A=	NCBI36
NG_011982.1:g.13464A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40771T=	ENSP00000514363.1:n.41-40771T=
ENST00000699403.1:c.61+40566T=	ENSP00000514364.1:n.61+40566T=
ENST00000465075.6:n.466A=
ENST00000466542.6:c.374A=	ENSP00000426627.1:p.His125=
ENST00000473530.6:n.555A=
ENST00000473712.6:n.396A=
ENST00000482226.2:n.353A=
ENST00000496692.6:n.470A=
ENST00000543859.5:c.371A=	ENSP00000444663.2:p.His124=
ENST00000611236.1:c.371A=	ENSP00000480953.1:p.His124=
NR_047648.1:n.473A=