Canonical Allele Identifier: CA1202800369

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589642_161589643delinsCG , CM000663.2:g.161589642_161589643delinsCG	GRCh38
NC_000001.10:g.161559432_161559433delinsCG , CM000663.1:g.161559432_161559433delinsCG	GRCh37
NC_000001.9:g.159826056_159826057delinsCG	NCBI36
NG_011982.1:g.13304_13305delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40612_41-40611delinsCG	ENSP00000514363.1:n.41-40612_41-40611delinsCG
ENST00000699403.1:c.61+40725_61+40726delinsCG	ENSP00000514364.1:n.61+40725_61+40726delinsCG
ENST00000465075.6:n.306_307delinsCG
ENST00000466542.6:c.214_215delinsCG	ENSP00000426627.1:p.Arg72=
ENST00000473530.6:n.395_396delinsCG
ENST00000473712.6:n.236_237delinsCG
ENST00000482226.2:n.193_194delinsCG
ENST00000496692.6:n.310_311delinsCG
ENST00000502411.5:n.511_512delinsCG
ENST00000543859.5:c.211_212delinsCG	ENSP00000444663.2:p.Arg71=
ENST00000611236.1:c.211_212delinsCG	ENSP00000480953.1:p.Arg71=
NR_047648.1:n.313_314delinsCG