Canonical Allele Identifier: CA343341888

Gene: FCGR2C

Linked Data

• gnomAD v3: 1-161589625-C-T
• gnomAD v4: 1-161589625-C-T
• MyVariant Identifiers: chr1:g.161559415C>T (hg19) ; chr1:g.161589625C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589625C>T , CM000663.2:g.161589625C>T	GRCh38
NC_000001.10:g.161559415C>T , CM000663.1:g.161559415C>T	GRCh37
NC_000001.9:g.159826039C>T	NCBI36
NG_011982.1:g.13287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40594G>A	ENSP00000514363.1:n.41-40594G>A
ENST00000699403.1:c.61+40743G>A	ENSP00000514364.1:n.61+40743G>A
ENST00000465075.6:n.289C>T
ENST00000466542.6:c.197C>T	ENSP00000426627.1:p.Ser66Phe
ENST00000473530.6:n.378C>T
ENST00000473712.6:n.219C>T
ENST00000482226.2:n.176C>T
ENST00000496692.6:n.293C>T
ENST00000502411.5:n.494C>T
ENST00000543859.5:c.194C>T	ENSP00000444663.2:p.Ser65Phe
ENST00000611236.1:c.194C>T	ENSP00000480953.1:p.Ser65Phe
NR_047648.1:n.296C>T