Canonical Allele Identifier: CA916324920

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1557868888
• gnomAD v3: 1-161589962-G-GT
• gnomAD v4: 1-161589962-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589962_161589963insT , CM000663.2:g.161589962_161589963insT	GRCh38
NC_000001.10:g.161559752_161559753insT , CM000663.1:g.161559752_161559753insT	GRCh37
NC_000001.9:g.159826376_159826377insT	NCBI36
NG_011982.1:g.13624_13625insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40932_41-40931insA	ENSP00000514363.1:n.41-40932_41-40931insA
ENST00000699403.1:c.61+40405_61+40406insA	ENSP00000514364.1:n.61+40405_61+40406insA
ENST00000465075.6:n.484-119_484-118insT
ENST00000466542.6:c.391+143_391+144insT	ENSP00000426627.1:n.391+143_391+144insT
ENST00000473530.6:n.572+143_572+144insT
ENST00000473712.6:n.413+143_413+144insT
ENST00000482226.2:n.370+143_370+144insT
ENST00000543859.5:c.388+143_388+144insT	ENSP00000444663.2:n.388+143_388+144insT
ENST00000611236.1:c.388+143_388+144insT	ENSP00000480953.1:n.388+143_388+144insT
NR_047648.1:n.490+143_490+144insT