Canonical Allele Identifier: CA343341937

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559426A>C (hg19) ; chr1:g.161589636A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589636A>C , CM000663.2:g.161589636A>C	GRCh38
NC_000001.10:g.161559426A>C , CM000663.1:g.161559426A>C	GRCh37
NC_000001.9:g.159826050A>C	NCBI36
NG_011982.1:g.13298A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40605T>G	ENSP00000514363.1:n.41-40605T>G
ENST00000699403.1:c.61+40732T>G	ENSP00000514364.1:n.61+40732T>G
ENST00000465075.6:n.300A>C
ENST00000466542.6:c.208A>C	ENSP00000426627.1:p.Thr70Pro
ENST00000473530.6:n.389A>C
ENST00000473712.6:n.230A>C
ENST00000482226.2:n.187A>C
ENST00000496692.6:n.304A>C
ENST00000502411.5:n.505A>C
ENST00000543859.5:c.205A>C	ENSP00000444663.2:p.Thr69Pro
ENST00000611236.1:c.205A>C	ENSP00000480953.1:p.Thr69Pro
NR_047648.1:n.307A>C