Canonical Allele Identifier: CA343343156

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559591C>A (hg19) ; chr1:g.161589801C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589801C>A , CM000663.2:g.161589801C>A	GRCh38
NC_000001.10:g.161559591C>A , CM000663.1:g.161559591C>A	GRCh37
NC_000001.9:g.159826215C>A	NCBI36
NG_011982.1:g.13463C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40770G>T	ENSP00000514363.1:n.41-40770G>T
ENST00000699403.1:c.61+40567G>T	ENSP00000514364.1:n.61+40567G>T
ENST00000465075.6:n.465C>A
ENST00000466542.6:c.373C>A	ENSP00000426627.1:p.His125Asn
ENST00000473530.6:n.554C>A
ENST00000473712.6:n.395C>A
ENST00000482226.2:n.352C>A
ENST00000496692.6:n.469C>A
ENST00000543859.5:c.370C>A	ENSP00000444663.2:p.His124Asn
ENST00000611236.1:c.370C>A	ENSP00000480953.1:p.His124Asn
NR_047648.1:n.472C>A