Canonical Allele Identifier: CA343342255

Gene: FCGR2C

Linked Data

• dbSNP Id: rs775686219
• gnomAD v3: 1-161589688-A-G
• gnomAD v4: 1-161589688-A-G
• MyVariant Identifiers: chr1:g.161559478A>G (hg19) ; chr1:g.161589688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589688A>G , CM000663.2:g.161589688A>G	GRCh38
NC_000001.10:g.161559478A>G , CM000663.1:g.161559478A>G	GRCh37
NC_000001.9:g.159826102A>G	NCBI36
NG_011982.1:g.13350A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40657T>C	ENSP00000514363.1:n.41-40657T>C
ENST00000699403.1:c.61+40680T>C	ENSP00000514364.1:n.61+40680T>C
ENST00000465075.6:n.352A>G
ENST00000466542.6:c.260A>G	ENSP00000426627.1:p.Asn87Ser
ENST00000473530.6:n.441A>G
ENST00000473712.6:n.282A>G
ENST00000482226.2:n.239A>G
ENST00000496692.6:n.356A>G
ENST00000502411.5:n.557A>G
ENST00000543859.5:c.257A>G	ENSP00000444663.2:p.Asn86Ser
ENST00000611236.1:c.257A>G	ENSP00000480953.1:p.Asn86Ser
NR_047648.1:n.359A>G