Canonical Allele Identifier: CA343343031

Gene: FCGR2C

Linked Data

• ClinVar Variation Id: 3094069
• ClinVar RCV Id: RCV004391423
• MyVariant Identifiers: chr1:g.161559576C>T (hg19) ; chr1:g.161589786C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589786C>T , CM000663.2:g.161589786C>T	GRCh38
NC_000001.10:g.161559576C>T , CM000663.1:g.161559576C>T	GRCh37
NC_000001.9:g.159826200C>T	NCBI36
NG_011982.1:g.13448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40755G>A	ENSP00000514363.1:n.41-40755G>A
ENST00000699403.1:c.61+40582G>A	ENSP00000514364.1:n.61+40582G>A
ENST00000465075.6:n.450C>T
ENST00000466542.6:c.358C>T	ENSP00000426627.1:p.Leu120Phe
ENST00000473530.6:n.539C>T
ENST00000473712.6:n.380C>T
ENST00000482226.2:n.337C>T
ENST00000496692.6:n.454C>T
ENST00000543859.5:c.355C>T	ENSP00000444663.2:p.Leu119Phe
ENST00000611236.1:c.355C>T	ENSP00000480953.1:p.Leu119Phe
NR_047648.1:n.457C>T