Canonical Allele Identifier: CA343342266

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559479T>G (hg19) ; chr1:g.161589689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589689T>G , CM000663.2:g.161589689T>G	GRCh38
NC_000001.10:g.161559479T>G , CM000663.1:g.161559479T>G	GRCh37
NC_000001.9:g.159826103T>G	NCBI36
NG_011982.1:g.13351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40658A>C	ENSP00000514363.1:n.41-40658A>C
ENST00000699403.1:c.61+40679A>C	ENSP00000514364.1:n.61+40679A>C
ENST00000465075.6:n.353T>G
ENST00000466542.6:c.261T>G	ENSP00000426627.1:p.Asn87Lys
ENST00000473530.6:n.442T>G
ENST00000473712.6:n.283T>G
ENST00000482226.2:n.240T>G
ENST00000496692.6:n.357T>G
ENST00000502411.5:n.558T>G
ENST00000543859.5:c.258T>G	ENSP00000444663.2:p.Asn86Lys
ENST00000611236.1:c.258T>G	ENSP00000480953.1:p.Asn86Lys
NR_047648.1:n.360T>G