Canonical Allele Identifier: CA1008413031
Gene: FCGR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161521126_161521133del , CM000663.2:g.161521126_161521133del GRCh38
NC_000001.10:g.161490916_161490923del , CM000663.1:g.161490916_161490923del GRCh37
NC_000001.9:g.159757540_159757547del NCBI36
NG_012066.1:g.20712_20719del
NG_012066.2:g.20712_20719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467525.5:c.918+1413_918+1420del ENSP00000476495.1:n.918+1413_918+1420del
ENST00000491841.1:n.425+1135_425+1142del
XM_011509287.1:c.*23+1135_*23+1142del XP_011507589.1:n.*23+1135_*23+1142del
XM_011509288.1:c.*23+1135_*23+1142del XP_011507590.1:n.*23+1135_*23+1142del
XM_011509289.1:c.*23+1135_*23+1142del XP_011507591.1:n.*23+1135_*23+1142del
XM_011509287.2:c.*23+1135_*23+1142del XP_011507589.1:n.*23+1135_*23+1142del
XM_017000664.1:c.944-2164_944-2157del XP_016856153.1:n.944-2164_944-2157del
XM_017000665.1:c.944-2164_944-2157del XP_016856154.1:n.944-2164_944-2157del
XR_001737042.1:n.1171+1135_1171+1142del