Canonical Allele Identifier: CA343343267

Gene: FCGR2C

Linked Data

• dbSNP Id: rs2102560139
• MyVariant Identifiers: chr1:g.161559604T>C (hg19) ; chr1:g.161589814T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589814T>C , CM000663.2:g.161589814T>C	GRCh38
NC_000001.10:g.161559604T>C , CM000663.1:g.161559604T>C	GRCh37
NC_000001.9:g.159826228T>C	NCBI36
NG_011982.1:g.13476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40783A>G	ENSP00000514363.1:n.41-40783A>G
ENST00000699403.1:c.61+40554A>G	ENSP00000514364.1:n.61+40554A>G
ENST00000465075.6:n.478T>C
ENST00000466542.6:c.386T>C	ENSP00000426627.1:p.Leu129Pro
ENST00000473530.6:n.567T>C
ENST00000473712.6:n.408T>C
ENST00000482226.2:n.365T>C
ENST00000496692.6:n.482T>C
ENST00000543859.5:c.383T>C	ENSP00000444663.2:p.Leu128Pro
ENST00000611236.1:c.383T>C	ENSP00000480953.1:p.Leu128Pro
NR_047648.1:n.485T>C