Canonical Allele Identifier: CA343342934

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559564G>T (hg19) ; chr1:g.161589774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589774G>T , CM000663.2:g.161589774G>T	GRCh38
NC_000001.10:g.161559564G>T , CM000663.1:g.161559564G>T	GRCh37
NC_000001.9:g.159826188G>T	NCBI36
NG_011982.1:g.13436G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40743C>A	ENSP00000514363.1:n.41-40743C>A
ENST00000699403.1:c.61+40594C>A	ENSP00000514364.1:n.61+40594C>A
ENST00000465075.6:n.438G>T
ENST00000466542.6:c.346G>T	ENSP00000426627.1:p.Gly116Cys
ENST00000473530.6:n.527G>T
ENST00000473712.6:n.368G>T
ENST00000482226.2:n.325G>T
ENST00000496692.6:n.442G>T
ENST00000543859.5:c.343G>T	ENSP00000444663.2:p.Gly115Cys
ENST00000611236.1:c.343G>T	ENSP00000480953.1:p.Gly115Cys
NR_047648.1:n.445G>T