Canonical Allele Identifier: CA1202800806

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589932_161589933delinsTG , CM000663.2:g.161589932_161589933delinsTG	GRCh38
NC_000001.10:g.161559722_161559723delinsTG , CM000663.1:g.161559722_161559723delinsTG	GRCh37
NC_000001.9:g.159826346_159826347delinsTG	NCBI36
NG_011982.1:g.13594_13595delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40902_41-40901delinsCA	ENSP00000514363.1:n.41-40902_41-40901delinsCA
ENST00000699403.1:c.61+40435_61+40436delinsCA	ENSP00000514364.1:n.61+40435_61+40436delinsCA
ENST00000465075.6:n.483+113_483+114delinsTG
ENST00000466542.6:c.391+113_391+114delinsTG	ENSP00000426627.1:n.391+113_391+114delinsTG
ENST00000473530.6:n.572+113_572+114delinsTG
ENST00000473712.6:n.413+113_413+114delinsTG
ENST00000482226.2:n.370+113_370+114delinsTG
ENST00000543859.5:c.388+113_388+114delinsTG	ENSP00000444663.2:n.388+113_388+114delinsTG
ENST00000611236.1:c.388+113_388+114delinsTG	ENSP00000480953.1:n.388+113_388+114delinsTG
NR_047648.1:n.490+113_490+114delinsTG