Canonical Allele Identifier: CA1211735

Gene: FCGR2C

Linked Data

• dbSNP Id: rs750874980
• ExAC: 1:161559638 C / T
• gnomAD v2: 1-161559638-C-T
• gnomAD v4: 1-161589848-C-T
• MyVariant Identifiers: chr1:g.161559638C>T (hg19) ; chr1:g.161589848C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589848C>T , CM000663.2:g.161589848C>T	GRCh38
NC_000001.10:g.161559638C>T , CM000663.1:g.161559638C>T	GRCh37
NC_000001.9:g.159826262C>T	NCBI36
NG_011982.1:g.13510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40817G>A	ENSP00000514363.1:n.41-40817G>A
ENST00000699403.1:c.61+40520G>A	ENSP00000514364.1:n.61+40520G>A
ENST00000465075.6:n.483+29C>T
ENST00000466542.6:c.391+29C>T	ENSP00000426627.1:n.391+29C>T
ENST00000473530.6:n.572+29C>T
ENST00000473712.6:n.413+29C>T
ENST00000482226.2:n.370+29C>T
ENST00000496692.6:n.516C>T
ENST00000543859.5:c.388+29C>T	ENSP00000444663.2:n.388+29C>T
ENST00000611236.1:c.388+29C>T	ENSP00000480953.1:n.388+29C>T
NR_047648.1:n.490+29C>T