Canonical Allele Identifier: CA343342976

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559569G>T (hg19) ; chr1:g.161589779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589779G>T , CM000663.2:g.161589779G>T	GRCh38
NC_000001.10:g.161559569G>T , CM000663.1:g.161559569G>T	GRCh37
NC_000001.9:g.159826193G>T	NCBI36
NG_011982.1:g.13441G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40748C>A	ENSP00000514363.1:n.41-40748C>A
ENST00000699403.1:c.61+40589C>A	ENSP00000514364.1:n.61+40589C>A
ENST00000465075.6:n.443G>T
ENST00000466542.6:c.351G>T	ENSP00000426627.1:p.Gln117His
ENST00000473530.6:n.532G>T
ENST00000473712.6:n.373G>T
ENST00000482226.2:n.330G>T
ENST00000496692.6:n.447G>T
ENST00000543859.5:c.348G>T	ENSP00000444663.2:p.Gln116His
ENST00000611236.1:c.348G>T	ENSP00000480953.1:p.Gln116His
NR_047648.1:n.450G>T