Canonical Allele Identifier: CA527135552

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1557868846
• gnomAD v2: 1-161559658-G-GA
• gnomAD v4: 1-161589868-G-GA
• MyVariant Identifiers: chr1:g.161559658_161559659insA (hg19) ; chr1:g.161589868_161589869insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589871dup , CM000663.2:g.161589871dup	GRCh38
NC_000001.10:g.161559661dup , CM000663.1:g.161559661dup	GRCh37
NC_000001.9:g.159826285dup	NCBI36
NG_011982.1:g.13533dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40838dup	ENSP00000514363.1:n.41-40838dup
ENST00000699403.1:c.61+40499dup	ENSP00000514364.1:n.61+40499dup
ENST00000465075.6:n.483+52dup
ENST00000466542.6:c.391+52dup	ENSP00000426627.1:n.391+52dup
ENST00000473530.6:n.572+52dup
ENST00000473712.6:n.413+52dup
ENST00000482226.2:n.370+52dup
ENST00000496692.6:n.539dup
ENST00000543859.5:c.388+52dup	ENSP00000444663.2:n.388+52dup
ENST00000611236.1:c.388+52dup	ENSP00000480953.1:n.388+52dup
NR_047648.1:n.490+52dup