Canonical Allele Identifier: CA2648792062

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589897-G-GCCACCCTCCTTTCCTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589897_161589898insCCACCCTCCTTTCCTGC , CM000663.2:g.161589897_161589898insCCACCCTCCTTTCCTGC	GRCh38
NC_000001.10:g.161559687_161559688insCCACCCTCCTTTCCTGC , CM000663.1:g.161559687_161559688insCCACCCTCCTTTCCTGC	GRCh37
NC_000001.9:g.159826311_159826312insCCACCCTCCTTTCCTGC	NCBI36
NG_011982.1:g.13559_13560insCCACCCTCCTTTCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40867_41-40866insGCAGGAAAGGAGGGTGG	ENSP00000514363.1:n.41-40867_41-40866insGCAGGAAAGGAGGGTGG
ENST00000699403.1:c.61+40470_61+40471insGCAGGAAAGGAGGGTGG	ENSP00000514364.1:n.61+40470_61+40471insGCAGGAAAGGAGGGTGG
ENST00000465075.6:n.483+78_483+79insCCACCCTCCTTTCCTGC
ENST00000466542.6:c.391+78_391+79insCCACCCTCCTTTCCTGC	ENSP00000426627.1:n.391+78_391+79insCCACCCTCCTTTCCTGC
ENST00000473530.6:n.572+78_572+79insCCACCCTCCTTTCCTGC
ENST00000473712.6:n.413+78_413+79insCCACCCTCCTTTCCTGC
ENST00000482226.2:n.370+78_370+79insCCACCCTCCTTTCCTGC
ENST00000543859.5:c.388+78_388+79insCCACCCTCCTTTCCTGC	ENSP00000444663.2:n.388+78_388+79insCCACCCTCCTTTCCTGC
ENST00000611236.1:c.388+78_388+79insCCACCCTCCTTTCCTGC	ENSP00000480953.1:n.388+78_388+79insCCACCCTCCTTTCCTGC
NR_047648.1:n.490+78_490+79insCCACCCTCCTTTCCTGC