Canonical Allele Identifier: CA527135549

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1286570225
• gnomAD v2: 1-161559583-ACC-A
• gnomAD v3: 1-161589793-ACC-A
• gnomAD v4: 1-161589793-ACC-A
• MyVariant Identifiers: chr1:g.161559584_161559585del (hg19) ; chr1:g.161589794_161589795del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589795_161589796del , CM000663.2:g.161589795_161589796del	GRCh38
NC_000001.10:g.161559585_161559586del , CM000663.1:g.161559585_161559586del	GRCh37
NC_000001.9:g.159826209_159826210del	NCBI36
NG_011982.1:g.13457_13458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40764_41-40763del	ENSP00000514363.1:n.41-40764_41-40763del
ENST00000699403.1:c.61+40573_61+40574del	ENSP00000514364.1:n.61+40573_61+40574del
ENST00000465075.6:n.459_460del
ENST00000466542.6:c.367_368del	ENSP00000426627.1:p.Pro123CysfsTer8
ENST00000473530.6:n.548_549del
ENST00000473712.6:n.389_390del
ENST00000482226.2:n.346_347del
ENST00000496692.6:n.463_464del
ENST00000543859.5:c.364_365del	ENSP00000444663.2:p.Pro122CysfsTer8
ENST00000611236.1:c.364_365del	ENSP00000480953.1:p.Pro122CysfsTer8
NR_047648.1:n.466_467del