Canonical Allele Identifier: CA1211678

Gene: FCGR2C

Linked Data

• dbSNP Id: rs749874298
• ExAC: 1:161559398 C / G
• gnomAD v2: 1-161559398-C-G
• gnomAD v3: 1-161589608-C-G
• gnomAD v4: 1-161589608-C-G
• MyVariant Identifiers: chr1:g.161559398C>G (hg19) ; chr1:g.161589608C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589608C>G , CM000663.2:g.161589608C>G	GRCh38
NC_000001.10:g.161559398C>G , CM000663.1:g.161559398C>G	GRCh37
NC_000001.9:g.159826022C>G	NCBI36
NG_011982.1:g.13270C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40577G>C	ENSP00000514363.1:n.41-40577G>C
ENST00000699403.1:c.61+40760G>C	ENSP00000514364.1:n.61+40760G>C
ENST00000465075.6:n.272C>G
ENST00000466542.6:c.180C>G	ENSP00000426627.1:p.Asn60Lys
ENST00000473530.6:n.361C>G
ENST00000473712.6:n.202C>G
ENST00000482226.2:n.159C>G
ENST00000496692.6:n.276C>G
ENST00000502411.5:n.477C>G
ENST00000543859.5:c.177C>G	ENSP00000444663.2:p.Asn59Lys
ENST00000611236.1:c.177C>G	ENSP00000480953.1:p.Asn59Lys
NR_047648.1:n.279C>G