Canonical Allele Identifier: CA343341926

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559423C>G (hg19) ; chr1:g.161589633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589633C>G , CM000663.2:g.161589633C>G	GRCh38
NC_000001.10:g.161559423C>G , CM000663.1:g.161559423C>G	GRCh37
NC_000001.9:g.159826047C>G	NCBI36
NG_011982.1:g.13295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40602G>C	ENSP00000514363.1:n.41-40602G>C
ENST00000699403.1:c.61+40735G>C	ENSP00000514364.1:n.61+40735G>C
ENST00000465075.6:n.297C>G
ENST00000466542.6:c.205C>G	ENSP00000426627.1:p.Leu69Val
ENST00000473530.6:n.386C>G
ENST00000473712.6:n.227C>G
ENST00000482226.2:n.184C>G
ENST00000496692.6:n.301C>G
ENST00000502411.5:n.502C>G
ENST00000543859.5:c.202C>G	ENSP00000444663.2:p.Leu68Val
ENST00000611236.1:c.202C>G	ENSP00000480953.1:p.Leu68Val
NR_047648.1:n.304C>G