Canonical Allele Identifier: CA343343295

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678464849
• MyVariant Identifiers: chr1:g.161559609G>C (hg19) ; chr1:g.161589819G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589819G>C , CM000663.2:g.161589819G>C	GRCh38
NC_000001.10:g.161559609G>C , CM000663.1:g.161559609G>C	GRCh37
NC_000001.9:g.159826233G>C	NCBI36
NG_011982.1:g.13481G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40788C>G	ENSP00000514363.1:n.41-40788C>G
ENST00000699403.1:c.61+40549C>G	ENSP00000514364.1:n.61+40549C>G
ENST00000465075.6:n.483G>C
ENST00000466542.6:c.391G>C	ENSP00000426627.1:p.Glu131Gln
ENST00000473530.6:n.572G>C
ENST00000473712.6:n.413G>C
ENST00000482226.2:n.370G>C
ENST00000496692.6:n.487G>C
ENST00000543859.5:c.388G>C	ENSP00000444663.2:p.Glu130Gln
ENST00000611236.1:c.388G>C	ENSP00000480953.1:p.Glu130Gln
NR_047648.1:n.490G>C