Canonical Allele Identifier: CA1143457787

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589750A= , CM000663.2:g.161589750A=	GRCh38
NC_000001.10:g.161559540A= , CM000663.1:g.161559540A=	GRCh37
NC_000001.9:g.159826164A=	NCBI36
NG_011982.1:g.13412A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40719T=	ENSP00000514363.1:n.41-40719T=
ENST00000699403.1:c.61+40618T=	ENSP00000514364.1:n.61+40618T=
ENST00000465075.6:n.414A=
ENST00000466542.6:c.322A=	ENSP00000426627.1:p.Ser108=
ENST00000473530.6:n.503A=
ENST00000473712.6:n.344A=
ENST00000482226.2:n.301A=
ENST00000496692.6:n.418A=
ENST00000543859.5:c.319A=	ENSP00000444663.2:p.Ser107=
ENST00000611236.1:c.319A=	ENSP00000480953.1:p.Ser107=
NR_047648.1:n.421A=