Canonical Allele Identifier: CA2648792052

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589608-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589608_161589609insA , CM000663.2:g.161589608_161589609insA	GRCh38
NC_000001.10:g.161559398_161559399insA , CM000663.1:g.161559398_161559399insA	GRCh37
NC_000001.9:g.159826022_159826023insA	NCBI36
NG_011982.1:g.13270_13271insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40578_41-40577insT	ENSP00000514363.1:n.41-40578_41-40577insT
ENST00000699403.1:c.61+40759_61+40760insT	ENSP00000514364.1:n.61+40759_61+40760insT
ENST00000465075.6:n.272_273insA
ENST00000466542.6:c.180_181insA	ENSP00000426627.1:p.Val61SerfsTer18
ENST00000473530.6:n.361_362insA
ENST00000473712.6:n.202_203insA
ENST00000482226.2:n.159_160insA
ENST00000496692.6:n.276_277insA
ENST00000502411.5:n.477_478insA
ENST00000543859.5:c.177_178insA	ENSP00000444663.2:p.Val60SerfsTer18
ENST00000611236.1:c.177_178insA	ENSP00000480953.1:p.Val60SerfsTer18
NR_047648.1:n.279_280insA