Canonical Allele Identifier: CA1008448834

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678467894
• gnomAD v3: 1-161589936-A-G
• gnomAD v4: 1-161589936-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589936A>G , CM000663.2:g.161589936A>G	GRCh38
NC_000001.10:g.161559726A>G , CM000663.1:g.161559726A>G	GRCh37
NC_000001.9:g.159826350A>G	NCBI36
NG_011982.1:g.13598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40905T>C	ENSP00000514363.1:n.41-40905T>C
ENST00000699403.1:c.61+40432T>C	ENSP00000514364.1:n.61+40432T>C
ENST00000465075.6:n.483+117A>G
ENST00000466542.6:c.391+117A>G	ENSP00000426627.1:n.391+117A>G
ENST00000473530.6:n.572+117A>G
ENST00000473712.6:n.413+117A>G
ENST00000482226.2:n.370+117A>G
ENST00000543859.5:c.388+117A>G	ENSP00000444663.2:n.388+117A>G
ENST00000611236.1:c.388+117A>G	ENSP00000480953.1:n.388+117A>G
NR_047648.1:n.490+117A>G