Canonical Allele Identifier: CA1202800763
Gene: FCGR2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589894C= , CM000663.2:g.161589894C= GRCh38
NC_000001.10:g.161559684C= , CM000663.1:g.161559684C= GRCh37
NC_000001.9:g.159826308C= NCBI36
NG_011982.1:g.13556C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40863G= ENSP00000514363.1:n.41-40863G=
ENST00000699403.1:c.61+40474G= ENSP00000514364.1:n.61+40474G=
ENST00000465075.6:n.483+75C=
ENST00000466542.6:c.391+75C= ENSP00000426627.1:n.391+75C=
ENST00000473530.6:n.572+75C=
ENST00000473712.6:n.413+75C=
ENST00000482226.2:n.370+75C=
ENST00000543859.5:c.388+75C= ENSP00000444663.2:n.388+75C=
ENST00000611236.1:c.388+75C= ENSP00000480953.1:n.388+75C=
NR_047648.1:n.490+75C=