Canonical Allele Identifier: CA421417419

Gene: FCGR2C

Linked Data

• dbSNP Id: rs780446500
• gnomAD v3: 1-161589782-C-T
• gnomAD v4: 1-161589782-C-T
• MyVariant Identifiers: chr1:g.161559572C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589782C>T , CM000663.2:g.161589782C>T	GRCh38
NC_000001.10:g.161559572C>T , CM000663.1:g.161559572C>T	GRCh37
NC_000001.9:g.159826196C>T	NCBI36
NG_011982.1:g.13444C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40751G>A	ENSP00000514363.1:n.41-40751G>A
ENST00000699403.1:c.61+40586G>A	ENSP00000514364.1:n.61+40586G>A
ENST00000465075.6:n.446C>T
ENST00000466542.6:c.354C>T	ENSP00000426627.1:p.Thr118=
ENST00000473530.6:n.535C>T
ENST00000473712.6:n.376C>T
ENST00000482226.2:n.333C>T
ENST00000496692.6:n.450C>T
ENST00000543859.5:c.351C>T	ENSP00000444663.2:p.Thr117=
ENST00000611236.1:c.351C>T	ENSP00000480953.1:p.Thr117=
NR_047648.1:n.453C>T