Canonical Allele Identifier: CA343342042

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559444A>C (hg19) ; chr1:g.161589654A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589654A>C , CM000663.2:g.161589654A>C	GRCh38
NC_000001.10:g.161559444A>C , CM000663.1:g.161559444A>C	GRCh37
NC_000001.9:g.159826068A>C	NCBI36
NG_011982.1:g.13316A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40623T>G	ENSP00000514363.1:n.41-40623T>G
ENST00000699403.1:c.61+40714T>G	ENSP00000514364.1:n.61+40714T>G
ENST00000465075.6:n.318A>C
ENST00000466542.6:c.226A>C	ENSP00000426627.1:p.Ser76Arg
ENST00000473530.6:n.407A>C
ENST00000473712.6:n.248A>C
ENST00000482226.2:n.205A>C
ENST00000496692.6:n.322A>C
ENST00000502411.5:n.523A>C
ENST00000543859.5:c.223A>C	ENSP00000444663.2:p.Ser75Arg
ENST00000611236.1:c.223A>C	ENSP00000480953.1:p.Ser75Arg
NR_047648.1:n.325A>C