Canonical Allele Identifier: CA421417435

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559599T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589809T>A , CM000663.2:g.161589809T>A	GRCh38
NC_000001.10:g.161559599T>A , CM000663.1:g.161559599T>A	GRCh37
NC_000001.9:g.159826223T>A	NCBI36
NG_011982.1:g.13471T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40778A>T	ENSP00000514363.1:n.41-40778A>T
ENST00000699403.1:c.61+40559A>T	ENSP00000514364.1:n.61+40559A>T
ENST00000465075.6:n.473T>A
ENST00000466542.6:c.381T>A	ENSP00000426627.1:p.Thr127=
ENST00000473530.6:n.562T>A
ENST00000473712.6:n.403T>A
ENST00000482226.2:n.360T>A
ENST00000496692.6:n.477T>A
ENST00000543859.5:c.378T>A	ENSP00000444663.2:p.Thr126=
ENST00000611236.1:c.378T>A	ENSP00000480953.1:p.Thr126=
NR_047648.1:n.480T>A