Canonical Allele Identifier: CA1202800837

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678468328
• gnomAD v4: 1-161589955-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589955A>T , CM000663.2:g.161589955A>T	GRCh38
NC_000001.10:g.161559745A>T , CM000663.1:g.161559745A>T	GRCh37
NC_000001.9:g.159826369A>T	NCBI36
NG_011982.1:g.13617A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40924T>A	ENSP00000514363.1:n.41-40924T>A
ENST00000699403.1:c.61+40413T>A	ENSP00000514364.1:n.61+40413T>A
ENST00000465075.6:n.484-126A>T
ENST00000466542.6:c.391+136A>T	ENSP00000426627.1:n.391+136A>T
ENST00000473530.6:n.572+136A>T
ENST00000473712.6:n.413+136A>T
ENST00000482226.2:n.370+136A>T
ENST00000543859.5:c.388+136A>T	ENSP00000444663.2:n.388+136A>T
ENST00000611236.1:c.388+136A>T	ENSP00000480953.1:n.388+136A>T
NR_047648.1:n.490+136A>T