Canonical Allele Identifier: CA421417437

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589812-G-A
• MyVariant Identifiers: chr1:g.161559602G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589812G>A , CM000663.2:g.161589812G>A	GRCh38
NC_000001.10:g.161559602G>A , CM000663.1:g.161559602G>A	GRCh37
NC_000001.9:g.159826226G>A	NCBI36
NG_011982.1:g.13474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40781C>T	ENSP00000514363.1:n.41-40781C>T
ENST00000699403.1:c.61+40556C>T	ENSP00000514364.1:n.61+40556C>T
ENST00000465075.6:n.476G>A
ENST00000466542.6:c.384G>A	ENSP00000426627.1:p.Val128=
ENST00000473530.6:n.565G>A
ENST00000473712.6:n.406G>A
ENST00000482226.2:n.363G>A
ENST00000496692.6:n.480G>A
ENST00000543859.5:c.381G>A	ENSP00000444663.2:p.Val127=
ENST00000611236.1:c.381G>A	ENSP00000480953.1:p.Val127=
NR_047648.1:n.483G>A