Canonical Allele Identifier: CA343342293

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589693-A-T
• MyVariant Identifiers: chr1:g.161559483A>T (hg19) ; chr1:g.161589693A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589693A>T , CM000663.2:g.161589693A>T	GRCh38
NC_000001.10:g.161559483A>T , CM000663.1:g.161559483A>T	GRCh37
NC_000001.9:g.159826107A>T	NCBI36
NG_011982.1:g.13355A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40662T>A	ENSP00000514363.1:n.41-40662T>A
ENST00000699403.1:c.61+40675T>A	ENSP00000514364.1:n.61+40675T>A
ENST00000465075.6:n.357A>T
ENST00000466542.6:c.265A>T	ENSP00000426627.1:p.Asn89Tyr
ENST00000473530.6:n.446A>T
ENST00000473712.6:n.287A>T
ENST00000482226.2:n.244A>T
ENST00000496692.6:n.361A>T
ENST00000502411.5:n.562A>T
ENST00000543859.5:c.262A>T	ENSP00000444663.2:p.Asn88Tyr
ENST00000611236.1:c.262A>T	ENSP00000480953.1:p.Asn88Tyr
NR_047648.1:n.364A>T