Canonical Allele Identifier: CA343342211

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678459345
• MyVariant Identifiers: chr1:g.161559471T>G (hg19) ; chr1:g.161589681T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589681T>G , CM000663.2:g.161589681T>G	GRCh38
NC_000001.10:g.161559471T>G , CM000663.1:g.161559471T>G	GRCh37
NC_000001.9:g.159826095T>G	NCBI36
NG_011982.1:g.13343T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40650A>C	ENSP00000514363.1:n.41-40650A>C
ENST00000699403.1:c.61+40687A>C	ENSP00000514364.1:n.61+40687A>C
ENST00000465075.6:n.345T>G
ENST00000466542.6:c.253T>G	ENSP00000426627.1:p.Phe85Val
ENST00000473530.6:n.434T>G
ENST00000473712.6:n.275T>G
ENST00000482226.2:n.232T>G
ENST00000496692.6:n.349T>G
ENST00000502411.5:n.550T>G
ENST00000543859.5:c.250T>G	ENSP00000444663.2:p.Phe84Val
ENST00000611236.1:c.250T>G	ENSP00000480953.1:p.Phe84Val
NR_047648.1:n.352T>G