Canonical Allele Identifier: CA343343196

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559593T>A (hg19) ; chr1:g.161589803T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589803T>A , CM000663.2:g.161589803T>A	GRCh38
NC_000001.10:g.161559593T>A , CM000663.1:g.161559593T>A	GRCh37
NC_000001.9:g.159826217T>A	NCBI36
NG_011982.1:g.13465T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40772A>T	ENSP00000514363.1:n.41-40772A>T
ENST00000699403.1:c.61+40565A>T	ENSP00000514364.1:n.61+40565A>T
ENST00000465075.6:n.467T>A
ENST00000466542.6:c.375T>A	ENSP00000426627.1:p.His125Gln
ENST00000473530.6:n.556T>A
ENST00000473712.6:n.397T>A
ENST00000482226.2:n.354T>A
ENST00000496692.6:n.471T>A
ENST00000543859.5:c.372T>A	ENSP00000444663.2:p.His124Gln
ENST00000611236.1:c.372T>A	ENSP00000480953.1:p.His124Gln
NR_047648.1:n.474T>A