Canonical Allele Identifier: CA343342161

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559463T>C (hg19) ; chr1:g.161589673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589673T>C , CM000663.2:g.161589673T>C	GRCh38
NC_000001.10:g.161559463T>C , CM000663.1:g.161559463T>C	GRCh37
NC_000001.9:g.159826087T>C	NCBI36
NG_011982.1:g.13335T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40642A>G	ENSP00000514363.1:n.41-40642A>G
ENST00000699403.1:c.61+40695A>G	ENSP00000514364.1:n.61+40695A>G
ENST00000465075.6:n.337T>C
ENST00000466542.6:c.245T>C	ENSP00000426627.1:p.Ile82Thr
ENST00000473530.6:n.426T>C
ENST00000473712.6:n.267T>C
ENST00000482226.2:n.224T>C
ENST00000496692.6:n.341T>C
ENST00000502411.5:n.542T>C
ENST00000543859.5:c.242T>C	ENSP00000444663.2:p.Ile81Thr
ENST00000611236.1:c.242T>C	ENSP00000480953.1:p.Ile81Thr
NR_047648.1:n.344T>C