Canonical Allele Identifier: CA343341795

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559399G>T (hg19) ; chr1:g.161589609G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589609G>T , CM000663.2:g.161589609G>T	GRCh38
NC_000001.10:g.161559399G>T , CM000663.1:g.161559399G>T	GRCh37
NC_000001.9:g.159826023G>T	NCBI36
NG_011982.1:g.13271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40578C>A	ENSP00000514363.1:n.41-40578C>A
ENST00000699403.1:c.61+40759C>A	ENSP00000514364.1:n.61+40759C>A
ENST00000465075.6:n.273G>T
ENST00000466542.6:c.181G>T	ENSP00000426627.1:p.Val61Leu
ENST00000473530.6:n.362G>T
ENST00000473712.6:n.203G>T
ENST00000482226.2:n.160G>T
ENST00000496692.6:n.277G>T
ENST00000502411.5:n.478G>T
ENST00000543859.5:c.178G>T	ENSP00000444663.2:p.Val60Leu
ENST00000611236.1:c.178G>T	ENSP00000480953.1:p.Val60Leu
NR_047648.1:n.280G>T