Canonical Allele Identifier: CA343341961

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589637-C-T
• MyVariant Identifiers: chr1:g.161559427C>T (hg19) ; chr1:g.161589637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589637C>T , CM000663.2:g.161589637C>T	GRCh38
NC_000001.10:g.161559427C>T , CM000663.1:g.161559427C>T	GRCh37
NC_000001.9:g.159826051C>T	NCBI36
NG_011982.1:g.13299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40606G>A	ENSP00000514363.1:n.41-40606G>A
ENST00000699403.1:c.61+40731G>A	ENSP00000514364.1:n.61+40731G>A
ENST00000465075.6:n.301C>T
ENST00000466542.6:c.209C>T	ENSP00000426627.1:p.Thr70Ile
ENST00000473530.6:n.390C>T
ENST00000473712.6:n.231C>T
ENST00000482226.2:n.188C>T
ENST00000496692.6:n.305C>T
ENST00000502411.5:n.506C>T
ENST00000543859.5:c.206C>T	ENSP00000444663.2:p.Thr69Ile
ENST00000611236.1:c.206C>T	ENSP00000480953.1:p.Thr69Ile
NR_047648.1:n.308C>T