Canonical Allele Identifier: CA343343232

Gene: FCGR2C

Linked Data

• COSMIC: COSN15658720
• MyVariant Identifiers: chr1:g.161559598C>T (hg19) ; chr1:g.161589808C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589808C>T , CM000663.2:g.161589808C>T	GRCh38
NC_000001.10:g.161559598C>T , CM000663.1:g.161559598C>T	GRCh37
NC_000001.9:g.159826222C>T	NCBI36
NG_011982.1:g.13470C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40777G>A	ENSP00000514363.1:n.41-40777G>A
ENST00000699403.1:c.61+40560G>A	ENSP00000514364.1:n.61+40560G>A
ENST00000465075.6:n.472C>T
ENST00000466542.6:c.380C>T	ENSP00000426627.1:p.Thr127Ile
ENST00000473530.6:n.561C>T
ENST00000473712.6:n.402C>T
ENST00000482226.2:n.359C>T
ENST00000496692.6:n.476C>T
ENST00000543859.5:c.377C>T	ENSP00000444663.2:p.Thr126Ile
ENST00000611236.1:c.377C>T	ENSP00000480953.1:p.Thr126Ile
NR_047648.1:n.479C>T