Canonical Allele Identifier: CA343342864

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559556G>T (hg19) ; chr1:g.161589766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589766G>T , CM000663.2:g.161589766G>T	GRCh38
NC_000001.10:g.161559556G>T , CM000663.1:g.161559556G>T	GRCh37
NC_000001.9:g.159826180G>T	NCBI36
NG_011982.1:g.13428G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40735C>A	ENSP00000514363.1:n.41-40735C>A
ENST00000699403.1:c.61+40602C>A	ENSP00000514364.1:n.61+40602C>A
ENST00000465075.6:n.430G>T
ENST00000466542.6:c.338G>T	ENSP00000426627.1:p.Cys113Phe
ENST00000473530.6:n.519G>T
ENST00000473712.6:n.360G>T
ENST00000482226.2:n.317G>T
ENST00000496692.6:n.434G>T
ENST00000543859.5:c.335G>T	ENSP00000444663.2:p.Cys112Phe
ENST00000611236.1:c.335G>T	ENSP00000480953.1:p.Cys112Phe
NR_047648.1:n.437G>T