Canonical Allele Identifier: CA1202785195

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544667G= , CM000663.2:g.161544667G=	GRCh38
NC_000001.10:g.161514457G= , CM000663.1:g.161514457G=	GRCh37
NC_000001.9:g.159781081G=	NCBI36
NG_009066.1:g.10957C= , LRG_60:g.10957C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367967.8:c.577+34C=	ENSP00000356944.3:n.577+34C=
ENST00000426740.8:c.574+34C=	ENSP00000410180.3:n.574+34C=
ENST00000436743.7:c.577+34C=	ENSP00000416607.1:n.577+34C=
ENST00000699395.1:c.577+34C=	ENSP00000514356.1:n.577+34C=
ENST00000699396.1:c.577+34C=	ENSP00000514357.1:n.577+34C=
ENST00000699397.1:c.577+34C=	ENSP00000514358.1:n.577+34C=
ENST00000699398.1:c.611C=	ENSP00000514359.1:p.Thr204=
ENST00000699399.1:c.526+34C=	ENSP00000514360.1:n.526+34C=
ENST00000699400.1:c.574+34C=	ENSP00000514361.1:n.574+34C=
ENST00000699401.1:c.611C=	ENSP00000514362.1:p.Thr204=
ENST00000426740.7:c.574+34C=	ENSP00000410180.3:n.574+34C=
ENST00000436743.6:c.577+34C=	ENSP00000416607.1:n.577+34C=
ENST00000443193.6:c.577+34C= MANE Select	ENSP00000392047.2:n.577+34C=
ENST00000367967.7:c.577+34C=	ENSP00000356944.3:n.577+34C=
ENST00000367969.7:c.685+34C=	ENSP00000356946.3:n.685+34C=
ENST00000426740.5:c.627+34C=
ENST00000436743.5:c.577+34C=	ENSP00000416607.1:n.577+34C=
ENST00000443193.5:c.577+34C=	ENSP00000392047.2:n.577+34C=
NM_000569.6:c.685+34C=	NP_000560.5:n.685+34C=
NM_001127592.1:c.682+34C=	NP_001121064.1:n.682+34C=
NM_001127593.1:c.577+34C= , LRG_60t1:c.577+34C=	NP_001121065.1:n.577+34C=
NM_001127595.1:c.577+34C=	NP_001121067.1:n.577+34C=
NM_001127596.1:c.574+34C=	NP_001121068.1:n.574+34C=
XM_011509293.1:c.428-1468C=	XP_011507595.1:n.428-1468C=
NM_000569.7:c.892+34C=	NP_000560.6:n.892+34C=
NM_001127592.2:c.889+34C=	NP_001121064.2:n.889+34C=
NM_001329120.1:c.577+34C=	NP_001316049.1:n.577+34C=
NM_001329122.1:c.635-1468C=	NP_001316051.1:n.635-1468C=
XM_024454064.1:c.574+34C=	XP_024309832.1:n.574+34C=
NM_001127595.2:c.577+34C=	NP_001121067.1:n.577+34C=
NM_001127596.2:c.574+34C=	NP_001121068.1:n.574+34C=
NM_000569.8:c.577+34C= MANE Select	NP_000560.7:n.577+34C=
NM_001329120.2:c.577+34C=	NP_001316049.1:n.577+34C=
NM_001386450.1:c.574+34C=	NP_001373379.1:n.574+34C=