Canonical Allele Identifier: CA343341864

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559411G>C (hg19) ; chr1:g.161589621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589621G>C , CM000663.2:g.161589621G>C	GRCh38
NC_000001.10:g.161559411G>C , CM000663.1:g.161559411G>C	GRCh37
NC_000001.9:g.159826035G>C	NCBI36
NG_011982.1:g.13283G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40590C>G	ENSP00000514363.1:n.41-40590C>G
ENST00000699403.1:c.61+40747C>G	ENSP00000514364.1:n.61+40747C>G
ENST00000465075.6:n.285G>C
ENST00000466542.6:c.193G>C	ENSP00000426627.1:p.Asp65His
ENST00000473530.6:n.374G>C
ENST00000473712.6:n.215G>C
ENST00000482226.2:n.172G>C
ENST00000496692.6:n.289G>C
ENST00000502411.5:n.490G>C
ENST00000543859.5:c.190G>C	ENSP00000444663.2:p.Asp64His
ENST00000611236.1:c.190G>C	ENSP00000480953.1:p.Asp64His
NR_047648.1:n.292G>C