Canonical Allele Identifier: CA343343248

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559601T>A (hg19) ; chr1:g.161589811T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589811T>A , CM000663.2:g.161589811T>A	GRCh38
NC_000001.10:g.161559601T>A , CM000663.1:g.161559601T>A	GRCh37
NC_000001.9:g.159826225T>A	NCBI36
NG_011982.1:g.13473T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40780A>T	ENSP00000514363.1:n.41-40780A>T
ENST00000699403.1:c.61+40557A>T	ENSP00000514364.1:n.61+40557A>T
ENST00000465075.6:n.475T>A
ENST00000466542.6:c.383T>A	ENSP00000426627.1:p.Val128Glu
ENST00000473530.6:n.564T>A
ENST00000473712.6:n.405T>A
ENST00000482226.2:n.362T>A
ENST00000496692.6:n.479T>A
ENST00000543859.5:c.380T>A	ENSP00000444663.2:p.Val127Glu
ENST00000611236.1:c.380T>A	ENSP00000480953.1:p.Val127Glu
NR_047648.1:n.482T>A