Canonical Allele Identifier: CA421417423

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559578C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589788C>T , CM000663.2:g.161589788C>T	GRCh38
NC_000001.10:g.161559578C>T , CM000663.1:g.161559578C>T	GRCh37
NC_000001.9:g.159826202C>T	NCBI36
NG_011982.1:g.13450C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40757G>A	ENSP00000514363.1:n.41-40757G>A
ENST00000699403.1:c.61+40580G>A	ENSP00000514364.1:n.61+40580G>A
ENST00000465075.6:n.452C>T
ENST00000466542.6:c.360C>T	ENSP00000426627.1:p.Leu120=
ENST00000473530.6:n.541C>T
ENST00000473712.6:n.382C>T
ENST00000482226.2:n.339C>T
ENST00000496692.6:n.456C>T
ENST00000543859.5:c.357C>T	ENSP00000444663.2:p.Leu119=
ENST00000611236.1:c.357C>T	ENSP00000480953.1:p.Leu119=
NR_047648.1:n.459C>T