Canonical Allele Identifier: CA343342269

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559480G>A (hg19) ; chr1:g.161589690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589690G>A , CM000663.2:g.161589690G>A	GRCh38
NC_000001.10:g.161559480G>A , CM000663.1:g.161559480G>A	GRCh37
NC_000001.9:g.159826104G>A	NCBI36
NG_011982.1:g.13352G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40659C>T	ENSP00000514363.1:n.41-40659C>T
ENST00000699403.1:c.61+40678C>T	ENSP00000514364.1:n.61+40678C>T
ENST00000465075.6:n.354G>A
ENST00000466542.6:c.262G>A	ENSP00000426627.1:p.Gly88Arg
ENST00000473530.6:n.443G>A
ENST00000473712.6:n.284G>A
ENST00000482226.2:n.241G>A
ENST00000496692.6:n.358G>A
ENST00000502411.5:n.559G>A
ENST00000543859.5:c.259G>A	ENSP00000444663.2:p.Gly87Arg
ENST00000611236.1:c.259G>A	ENSP00000480953.1:p.Gly87Arg
NR_047648.1:n.361G>A