Canonical Allele Identifier: CA1211703

Gene: FCGR2C

Linked Data

• ClinVar Variation Id: 2595001
• ClinVar RCV Id: RCV004338071
• dbSNP Id: rs187810534
• ExAC: 1:161559502 C / T
• gnomAD v2: 1-161559502-C-T
• gnomAD v3: 1-161589712-C-T
• gnomAD v4: 1-161589712-C-T
• MyVariant Identifiers: chr1:g.161559502C>T (hg19) ; chr1:g.161589712C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589712C>T , CM000663.2:g.161589712C>T	GRCh38
NC_000001.10:g.161559502C>T , CM000663.1:g.161559502C>T	GRCh37
NC_000001.9:g.159826126C>T	NCBI36
NG_011982.1:g.13374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40681G>A	ENSP00000514363.1:n.41-40681G>A
ENST00000699403.1:c.61+40656G>A	ENSP00000514364.1:n.61+40656G>A
ENST00000465075.6:n.376C>T
ENST00000466542.6:c.284C>T	ENSP00000426627.1:p.Thr95Met
ENST00000473530.6:n.465C>T
ENST00000473712.6:n.306C>T
ENST00000482226.2:n.263C>T
ENST00000496692.6:n.380C>T
ENST00000543859.5:c.281C>T	ENSP00000444663.2:p.Thr94Met
ENST00000611236.1:c.281C>T	ENSP00000480953.1:p.Thr94Met
NR_047648.1:n.383C>T