Canonical Allele Identifier: CA890206272

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1408779449
• gnomAD v3: 1-161589900-A-C
• gnomAD v4: 1-161589900-A-C
• MyVariant Identifiers: chr1:g.161559690A>C (hg19) ; chr1:g.161589900A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589900A>C , CM000663.2:g.161589900A>C	GRCh38
NC_000001.10:g.161559690A>C , CM000663.1:g.161559690A>C	GRCh37
NC_000001.9:g.159826314A>C	NCBI36
NG_011982.1:g.13562A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40869T>G	ENSP00000514363.1:n.41-40869T>G
ENST00000699403.1:c.61+40468T>G	ENSP00000514364.1:n.61+40468T>G
ENST00000465075.6:n.483+81A>C
ENST00000466542.6:c.391+81A>C	ENSP00000426627.1:n.391+81A>C
ENST00000473530.6:n.572+81A>C
ENST00000473712.6:n.413+81A>C
ENST00000482226.2:n.370+81A>C
ENST00000543859.5:c.388+81A>C	ENSP00000444663.2:n.388+81A>C
ENST00000611236.1:c.388+81A>C	ENSP00000480953.1:n.388+81A>C
NR_047648.1:n.490+81A>C