Canonical Allele Identifier: CA343342824

Gene: FCGR2C

Linked Data

• dbSNP Id: rs574231211
• gnomAD v3: 1-161589763-C-A
• gnomAD v4: 1-161589763-C-A
• MyVariant Identifiers: chr1:g.161559553C>A (hg19) ; chr1:g.161589763C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589763C>A , CM000663.2:g.161589763C>A	GRCh38
NC_000001.10:g.161559553C>A , CM000663.1:g.161559553C>A	GRCh37
NC_000001.9:g.159826177C>A	NCBI36
NG_011982.1:g.13425C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40732G>T	ENSP00000514363.1:n.41-40732G>T
ENST00000699403.1:c.61+40605G>T	ENSP00000514364.1:n.61+40605G>T
ENST00000465075.6:n.427C>A
ENST00000466542.6:c.335C>A	ENSP00000426627.1:p.Thr112Lys
ENST00000473530.6:n.516C>A
ENST00000473712.6:n.357C>A
ENST00000482226.2:n.314C>A
ENST00000496692.6:n.431C>A
ENST00000543859.5:c.332C>A	ENSP00000444663.2:p.Thr111Lys
ENST00000611236.1:c.332C>A	ENSP00000480953.1:p.Thr111Lys
NR_047648.1:n.434C>A