Canonical Allele Identifier: CA1147179471
Gene: FCGR2C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589929C= , CM000663.2:g.161589929C= GRCh38
NC_000001.10:g.161559719C= , CM000663.1:g.161559719C= GRCh37
NC_000001.9:g.159826343C= NCBI36
NG_011982.1:g.13591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40898G= ENSP00000514363.1:n.41-40898G=
ENST00000699403.1:c.61+40439G= ENSP00000514364.1:n.61+40439G=
ENST00000465075.6:n.483+110C=
ENST00000466542.6:c.391+110C= ENSP00000426627.1:n.391+110C=
ENST00000473530.6:n.572+110C=
ENST00000473712.6:n.413+110C=
ENST00000482226.2:n.370+110C=
ENST00000543859.5:c.388+110C= ENSP00000444663.2:n.388+110C=
ENST00000611236.1:c.388+110C= ENSP00000480953.1:n.388+110C=
NR_047648.1:n.490+110C=
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