Canonical Allele Identifier: CA1202800850

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678468704

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589969C>T , CM000663.2:g.161589969C>T	GRCh38
NC_000001.10:g.161559759C>T , CM000663.1:g.161559759C>T	GRCh37
NC_000001.9:g.159826383C>T	NCBI36
NG_011982.1:g.13631C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40938G>A	ENSP00000514363.1:n.41-40938G>A
ENST00000699403.1:c.61+40399G>A	ENSP00000514364.1:n.61+40399G>A
ENST00000465075.6:n.484-112C>T
ENST00000466542.6:c.391+150C>T	ENSP00000426627.1:n.391+150C>T
ENST00000473530.6:n.572+150C>T
ENST00000473712.6:n.413+150C>T
ENST00000482226.2:n.370+150C>T
ENST00000543859.5:c.388+150C>T	ENSP00000444663.2:n.388+150C>T
ENST00000611236.1:c.388+150C>T	ENSP00000480953.1:n.388+150C>T
NR_047648.1:n.490+150C>T