Canonical Allele Identifier: CA343342214

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559472T>G (hg19) ; chr1:g.161589682T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589682T>G , CM000663.2:g.161589682T>G	GRCh38
NC_000001.10:g.161559472T>G , CM000663.1:g.161559472T>G	GRCh37
NC_000001.9:g.159826096T>G	NCBI36
NG_011982.1:g.13344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40651A>C	ENSP00000514363.1:n.41-40651A>C
ENST00000699403.1:c.61+40686A>C	ENSP00000514364.1:n.61+40686A>C
ENST00000465075.6:n.346T>G
ENST00000466542.6:c.254T>G	ENSP00000426627.1:p.Phe85Cys
ENST00000473530.6:n.435T>G
ENST00000473712.6:n.276T>G
ENST00000482226.2:n.233T>G
ENST00000496692.6:n.350T>G
ENST00000502411.5:n.551T>G
ENST00000543859.5:c.251T>G	ENSP00000444663.2:p.Phe84Cys
ENST00000611236.1:c.251T>G	ENSP00000480953.1:p.Phe84Cys
NR_047648.1:n.353T>G