Canonical Allele Identifier: CA1211726

Gene: FCGR2C

Linked Data

• dbSNP Id: rs750413354
• ExAC: 1:161559598 CTG / C
• gnomAD v2: 1-161559598-CTG-C
• gnomAD v3: 1-161589808-CTG-C
• gnomAD v4: 1-161589808-CTG-C
• MyVariant Identifiers: chr1:g.161559599_161559600del (hg19) ; chr1:g.161589809_161589810del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589811_161589812del , CM000663.2:g.161589811_161589812del	GRCh38
NC_000001.10:g.161559601_161559602del , CM000663.1:g.161559601_161559602del	GRCh37
NC_000001.9:g.159826225_159826226del	NCBI36
NG_011982.1:g.13473_13474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40779_41-40778del	ENSP00000514363.1:n.41-40779_41-40778del
ENST00000699403.1:c.61+40558_61+40559del	ENSP00000514364.1:n.61+40558_61+40559del
ENST00000465075.6:n.475_476del
ENST00000466542.6:c.383_384del	ENSP00000426627.1:p.Val128AlafsTer3
ENST00000473530.6:n.564_565del
ENST00000473712.6:n.405_406del
ENST00000482226.2:n.362_363del
ENST00000496692.6:n.479_480del
ENST00000543859.5:c.380_381del	ENSP00000444663.2:p.Val127AlafsTer3
ENST00000611236.1:c.380_381del	ENSP00000480953.1:p.Val127AlafsTer3
NR_047648.1:n.482_483del