Canonical Allele Identifier: CA343343004

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1226449499
• gnomAD v2: 1-161559574-G-A
• gnomAD v3: 1-161589784-G-A
• gnomAD v4: 1-161589784-G-A
• MyVariant Identifiers: chr1:g.161559574G>A (hg19) ; chr1:g.161589784G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589784G>A , CM000663.2:g.161589784G>A	GRCh38
NC_000001.10:g.161559574G>A , CM000663.1:g.161559574G>A	GRCh37
NC_000001.9:g.159826198G>A	NCBI36
NG_011982.1:g.13446G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40753C>T	ENSP00000514363.1:n.41-40753C>T
ENST00000699403.1:c.61+40584C>T	ENSP00000514364.1:n.61+40584C>T
ENST00000465075.6:n.448G>A
ENST00000466542.6:c.356G>A	ENSP00000426627.1:p.Ser119Asn
ENST00000473530.6:n.537G>A
ENST00000473712.6:n.378G>A
ENST00000482226.2:n.335G>A
ENST00000496692.6:n.452G>A
ENST00000543859.5:c.353G>A	ENSP00000444663.2:p.Ser118Asn
ENST00000611236.1:c.353G>A	ENSP00000480953.1:p.Ser118Asn
NR_047648.1:n.455G>A