Canonical Allele Identifier: CA1211687

Gene: FCGR2C

Linked Data

• dbSNP Id: rs370539109
• ExAC: 1:161559432 C / T
• gnomAD v2: 1-161559432-C-T
• gnomAD v3: 1-161589642-C-T
• gnomAD v4: 1-161589642-C-T
• MyVariant Identifiers: chr1:g.161559432C>T (hg19) ; chr1:g.161559432_161559433delinsTG (hg19) ; chr1:g.161589642C>T (hg38) ; chr1:g.161589642_161589643delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589642C>T , CM000663.2:g.161589642C>T	GRCh38
NC_000001.10:g.161559432C>T , CM000663.1:g.161559432C>T	GRCh37
NC_000001.9:g.159826056C>T	NCBI36
NG_011982.1:g.13304C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40611G>A	ENSP00000514363.1:n.41-40611G>A
ENST00000699403.1:c.61+40726G>A	ENSP00000514364.1:n.61+40726G>A
ENST00000465075.6:n.306C>T
ENST00000466542.6:c.214C>T	ENSP00000426627.1:p.Arg72Trp
ENST00000473530.6:n.395C>T
ENST00000473712.6:n.236C>T
ENST00000482226.2:n.193C>T
ENST00000496692.6:n.310C>T
ENST00000502411.5:n.511C>T
ENST00000543859.5:c.211C>T	ENSP00000444663.2:p.Arg71Trp
ENST00000611236.1:c.211C>T	ENSP00000480953.1:p.Arg71Trp
NR_047648.1:n.313C>T