Canonical Allele Identifier: CA2648792109

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589962-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589962G>T , CM000663.2:g.161589962G>T	GRCh38
NC_000001.10:g.161559752G>T , CM000663.1:g.161559752G>T	GRCh37
NC_000001.9:g.159826376G>T	NCBI36
NG_011982.1:g.13624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40931C>A	ENSP00000514363.1:n.41-40931C>A
ENST00000699403.1:c.61+40406C>A	ENSP00000514364.1:n.61+40406C>A
ENST00000465075.6:n.484-119G>T
ENST00000466542.6:c.391+143G>T	ENSP00000426627.1:n.391+143G>T
ENST00000473530.6:n.572+143G>T
ENST00000473712.6:n.413+143G>T
ENST00000482226.2:n.370+143G>T
ENST00000543859.5:c.388+143G>T	ENSP00000444663.2:n.388+143G>T
ENST00000611236.1:c.388+143G>T	ENSP00000480953.1:n.388+143G>T
NR_047648.1:n.490+143G>T