Canonical Allele Identifier: CA343342343

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1332851479
• gnomAD v2: 1-161559495-A-G
• gnomAD v4: 1-161589705-A-G
• MyVariant Identifiers: chr1:g.161559495A>G (hg19) ; chr1:g.161589705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589705A>G , CM000663.2:g.161589705A>G	GRCh38
NC_000001.10:g.161559495A>G , CM000663.1:g.161559495A>G	GRCh37
NC_000001.9:g.159826119A>G	NCBI36
NG_011982.1:g.13367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40674T>C	ENSP00000514363.1:n.41-40674T>C
ENST00000699403.1:c.61+40663T>C	ENSP00000514364.1:n.61+40663T>C
ENST00000465075.6:n.369A>G
ENST00000466542.6:c.277A>G	ENSP00000426627.1:p.Thr93Ala
ENST00000473530.6:n.458A>G
ENST00000473712.6:n.299A>G
ENST00000482226.2:n.256A>G
ENST00000496692.6:n.373A>G
ENST00000543859.5:c.274A>G	ENSP00000444663.2:p.Thr92Ala
ENST00000611236.1:c.274A>G	ENSP00000480953.1:p.Thr92Ala
NR_047648.1:n.376A>G