Canonical Allele Identifier: CA1147183560

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589794C= , CM000663.2:g.161589794C=	GRCh38
NC_000001.10:g.161559584C= , CM000663.1:g.161559584C=	GRCh37
NC_000001.9:g.159826208C=	NCBI36
NG_011982.1:g.13456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40763G=	ENSP00000514363.1:n.41-40763G=
ENST00000699403.1:c.61+40574G=	ENSP00000514364.1:n.61+40574G=
ENST00000465075.6:n.458C=
ENST00000466542.6:c.366C=	ENSP00000426627.1:p.Asp122=
ENST00000473530.6:n.547C=
ENST00000473712.6:n.388C=
ENST00000482226.2:n.345C=
ENST00000496692.6:n.462C=
ENST00000543859.5:c.363C=	ENSP00000444663.2:p.Asp121=
ENST00000611236.1:c.363C=	ENSP00000480953.1:p.Asp121=
NR_047648.1:n.465C=