Canonical Allele Identifier: CA2531560034
Gene: FCGR2C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589887A>G , CM000663.2:g.161589887A>G GRCh38
NC_000001.10:g.161559677A>G , CM000663.1:g.161559677A>G GRCh37
NC_000001.9:g.159826301A>G NCBI36
NG_011982.1:g.13549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40856T>C ENSP00000514363.1:n.41-40856T>C
ENST00000699403.1:c.61+40481T>C ENSP00000514364.1:n.61+40481T>C
ENST00000465075.6:n.483+68A>G
ENST00000466542.6:c.391+68A>G ENSP00000426627.1:n.391+68A>G
ENST00000473530.6:n.572+68A>G
ENST00000473712.6:n.413+68A>G
ENST00000482226.2:n.370+68A>G
ENST00000543859.5:c.388+68A>G ENSP00000444663.2:n.388+68A>G
ENST00000611236.1:c.388+68A>G ENSP00000480953.1:n.388+68A>G
NR_047648.1:n.490+68A>G