Canonical Allele Identifier: CA1147983545

Gene: FCGR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161521110G= , CM000663.2:g.161521110G=	GRCh38
NC_000001.10:g.161490900G= , CM000663.1:g.161490900G=	GRCh37
NC_000001.9:g.159757524G=	NCBI36
NG_012066.1:g.20696G=
NG_012066.2:g.20696G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467525.5:c.918+1397G=	ENSP00000476495.1:n.918+1397G=
ENST00000491841.1:n.425+1119G=
XM_011509287.1:c.*23+1119G=	XP_011507589.1:n.*23+1119G=
XM_011509288.1:c.*23+1119G=	XP_011507590.1:n.*23+1119G=
XM_011509289.1:c.*23+1119G=	XP_011507591.1:n.*23+1119G=
XM_011509287.2:c.*23+1119G=	XP_011507589.1:n.*23+1119G=
XM_017000664.1:c.944-2180G=	XP_016856153.1:n.944-2180G=
XM_017000665.1:c.944-2180G=	XP_016856154.1:n.944-2180G=
XR_001737042.1:n.1171+1119G=