Canonical Allele Identifier: CA343342134

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559457A>G (hg19) ; chr1:g.161589667A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589667A>G , CM000663.2:g.161589667A>G	GRCh38
NC_000001.10:g.161559457A>G , CM000663.1:g.161559457A>G	GRCh37
NC_000001.9:g.159826081A>G	NCBI36
NG_011982.1:g.13329A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40636T>C	ENSP00000514363.1:n.41-40636T>C
ENST00000699403.1:c.61+40701T>C	ENSP00000514364.1:n.61+40701T>C
ENST00000465075.6:n.331A>G
ENST00000466542.6:c.239A>G	ENSP00000426627.1:p.Asp80Gly
ENST00000473530.6:n.420A>G
ENST00000473712.6:n.261A>G
ENST00000482226.2:n.218A>G
ENST00000496692.6:n.335A>G
ENST00000502411.5:n.536A>G
ENST00000543859.5:c.236A>G	ENSP00000444663.2:p.Asp79Gly
ENST00000611236.1:c.236A>G	ENSP00000480953.1:p.Asp79Gly
NR_047648.1:n.338A>G