Canonical Allele Identifier: CA2574078671
Gene: FCGR2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589953T>A , CM000663.2:g.161589953T>A GRCh38
NC_000001.10:g.161559743T>A , CM000663.1:g.161559743T>A GRCh37
NC_000001.9:g.159826367T>A NCBI36
NG_011982.1:g.13615T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40922A>T ENSP00000514363.1:n.41-40922A>T
ENST00000699403.1:c.61+40415A>T ENSP00000514364.1:n.61+40415A>T
ENST00000465075.6:n.484-128T>A
ENST00000466542.6:c.391+134T>A ENSP00000426627.1:n.391+134T>A
ENST00000473530.6:n.572+134T>A
ENST00000473712.6:n.413+134T>A
ENST00000482226.2:n.370+134T>A
ENST00000543859.5:c.388+134T>A ENSP00000444663.2:n.388+134T>A
ENST00000611236.1:c.388+134T>A ENSP00000480953.1:n.388+134T>A
NR_047648.1:n.490+134T>A