Canonical Allele Identifier: CA2648792124

Gene: FCGR2C

Linked Data

• dbSNP Id: rs2102560309
• gnomAD v4: 1-161589976-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589976C>G , CM000663.2:g.161589976C>G	GRCh38
NC_000001.10:g.161559766C>G , CM000663.1:g.161559766C>G	GRCh37
NC_000001.9:g.159826390C>G	NCBI36
NG_011982.1:g.13638C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40945G>C	ENSP00000514363.1:n.41-40945G>C
ENST00000699403.1:c.61+40392G>C	ENSP00000514364.1:n.61+40392G>C
ENST00000465075.6:n.484-105C>G
ENST00000466542.6:c.391+157C>G	ENSP00000426627.1:n.391+157C>G
ENST00000473530.6:n.572+157C>G
ENST00000473712.6:n.413+157C>G
ENST00000482226.2:n.370+157C>G
ENST00000543859.5:c.388+157C>G	ENSP00000444663.2:n.388+157C>G
ENST00000611236.1:c.388+157C>G	ENSP00000480953.1:n.388+157C>G
NR_047648.1:n.490+157C>G