Canonical Allele Identifier: CA890206269

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1402483379
• gnomAD v4: 1-161589898-A-G
• MyVariant Identifiers: chr1:g.161559688A>G (hg19) ; chr1:g.161589898A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589898A>G , CM000663.2:g.161589898A>G	GRCh38
NC_000001.10:g.161559688A>G , CM000663.1:g.161559688A>G	GRCh37
NC_000001.9:g.159826312A>G	NCBI36
NG_011982.1:g.13560A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40867T>C	ENSP00000514363.1:n.41-40867T>C
ENST00000699403.1:c.61+40470T>C	ENSP00000514364.1:n.61+40470T>C
ENST00000465075.6:n.483+79A>G
ENST00000466542.6:c.391+79A>G	ENSP00000426627.1:n.391+79A>G
ENST00000473530.6:n.572+79A>G
ENST00000473712.6:n.413+79A>G
ENST00000482226.2:n.370+79A>G
ENST00000543859.5:c.388+79A>G	ENSP00000444663.2:n.388+79A>G
ENST00000611236.1:c.388+79A>G	ENSP00000480953.1:n.388+79A>G
NR_047648.1:n.490+79A>G