Canonical Allele Identifier: CA2648792085
Gene: FCGR2C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589934_161589935insCACAGC , CM000663.2:g.161589934_161589935insCACAGC GRCh38
NC_000001.10:g.161559724_161559725insCACAGC , CM000663.1:g.161559724_161559725insCACAGC GRCh37
NC_000001.9:g.159826348_159826349insCACAGC NCBI36
NG_011982.1:g.13596_13597insCACAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40904_41-40903insGCTGTG ENSP00000514363.1:n.41-40904_41-40903insGCTGTG
ENST00000699403.1:c.61+40433_61+40434insGCTGTG ENSP00000514364.1:n.61+40433_61+40434insGCTGTG
ENST00000465075.6:n.483+115_483+116insCACAGC
ENST00000466542.6:c.391+115_391+116insCACAGC ENSP00000426627.1:n.391+115_391+116insCACAGC
ENST00000473530.6:n.572+115_572+116insCACAGC
ENST00000473712.6:n.413+115_413+116insCACAGC
ENST00000482226.2:n.370+115_370+116insCACAGC
ENST00000543859.5:c.388+115_388+116insCACAGC ENSP00000444663.2:n.388+115_388+116insCACAGC
ENST00000611236.1:c.388+115_388+116insCACAGC ENSP00000480953.1:n.388+115_388+116insCACAGC
NR_047648.1:n.490+115_490+116insCACAGC