Canonical Allele Identifier: CA1211702

Gene: FCGR2C

Linked Data

• dbSNP Id: rs760929449
• ExAC: 1:161559485 T / A
• gnomAD v3: 1-161589695-T-A
• gnomAD v4: 1-161589695-T-A
• MyVariant Identifiers: chr1:g.161559485T>A (hg19) ; chr1:g.161589695T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589695T>A , CM000663.2:g.161589695T>A	GRCh38
NC_000001.10:g.161559485T>A , CM000663.1:g.161559485T>A	GRCh37
NC_000001.9:g.159826109T>A	NCBI36
NG_011982.1:g.13357T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40664A>T	ENSP00000514363.1:n.41-40664A>T
ENST00000699403.1:c.61+40673A>T	ENSP00000514364.1:n.61+40673A>T
ENST00000465075.6:n.359T>A
ENST00000466542.6:c.267T>A	ENSP00000426627.1:p.Asn89Lys
ENST00000473530.6:n.448T>A
ENST00000473712.6:n.289T>A
ENST00000482226.2:n.246T>A
ENST00000496692.6:n.363T>A
ENST00000502411.5:n.564T>A
ENST00000543859.5:c.264T>A	ENSP00000444663.2:p.Asn88Lys
ENST00000611236.1:c.264T>A	ENSP00000480953.1:p.Asn88Lys
NR_047648.1:n.366T>A