Canonical Allele Identifier: CA1202800662

Gene: FCGR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589822_161589823delinsCA , CM000663.2:g.161589822_161589823delinsCA	GRCh38
NC_000001.10:g.161559612_161559613delinsCA , CM000663.1:g.161559612_161559613delinsCA	GRCh37
NC_000001.9:g.159826236_159826237delinsCA	NCBI36
NG_011982.1:g.13484_13485delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40792_41-40791delinsTG	ENSP00000514363.1:n.41-40792_41-40791delinsTG
ENST00000699403.1:c.61+40545_61+40546delinsTG	ENSP00000514364.1:n.61+40545_61+40546delinsTG
ENST00000465075.6:n.483+3_483+4delinsCA
ENST00000466542.6:c.391+3_391+4delinsCA	ENSP00000426627.1:n.391+3_391+4delinsCA
ENST00000473530.6:n.572+3_572+4delinsCA
ENST00000473712.6:n.413+3_413+4delinsCA
ENST00000482226.2:n.370+3_370+4delinsCA
ENST00000496692.6:n.490_491delinsCA
ENST00000543859.5:c.388+3_388+4delinsCA	ENSP00000444663.2:n.388+3_388+4delinsCA
ENST00000611236.1:c.388+3_388+4delinsCA	ENSP00000480953.1:n.388+3_388+4delinsCA
NR_047648.1:n.490+3_490+4delinsCA