Canonical Allele Identifier: CA421612608

Gene: FCGR3A

Linked Data

• MyVariant Identifiers: chr1:g.161514648T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544858T>G , CM000663.2:g.161544858T>G	GRCh38
NC_000001.10:g.161514648T>G , CM000663.1:g.161514648T>G	GRCh37
NC_000001.9:g.159781272T>G	NCBI36
NG_009066.1:g.10766A>C , LRG_60:g.10766A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.420A>C	ENSP00000356944.3:p.Thr140=
ENST00000426740.8:c.417A>C	ENSP00000410180.3:p.Thr139=
ENST00000436743.7:c.420A>C	ENSP00000416607.1:p.Thr140=
ENST00000699395.1:c.420A>C	ENSP00000514356.1:p.Thr140=
ENST00000699396.1:c.420A>C	ENSP00000514357.1:p.Thr140=
ENST00000699397.1:c.420A>C	ENSP00000514358.1:p.Thr140=
ENST00000699398.1:c.420A>C	ENSP00000514359.1:p.Thr140=
ENST00000699399.1:c.369A>C	ENSP00000514360.1:p.Thr123=
ENST00000699400.1:c.417A>C	ENSP00000514361.1:p.Thr139=
ENST00000699401.1:c.420A>C	ENSP00000514362.1:p.Thr140=
ENST00000699402.1:c.417A>C	ENSP00000514363.1:p.Thr139=
ENST00000426740.7:c.417A>C	ENSP00000410180.3:p.Thr139=
ENST00000436743.6:c.420A>C	ENSP00000416607.1:p.Thr140=
ENST00000443193.6:c.420A>C MANE Select	ENSP00000392047.2:p.Thr140=
ENST00000367967.7:c.420A>C	ENSP00000356944.3:p.Thr140=
ENST00000367969.7:c.528A>C	ENSP00000356946.3:p.Thr176=
ENST00000426740.5:c.470A>C
ENST00000436743.5:c.420A>C	ENSP00000416607.1:p.Thr140=
ENST00000443193.5:c.420A>C	ENSP00000392047.2:p.Thr140=
NM_000569.6:c.528A>C	NP_000560.5:p.Thr176=
NM_001127592.1:c.525A>C	NP_001121064.1:p.Thr175=
NM_001127593.1:c.420A>C , LRG_60t1:c.420A>C	NP_001121065.1:p.Thr140=
NM_001127595.1:c.420A>C	NP_001121067.1:p.Thr140=
NM_001127596.1:c.417A>C	NP_001121068.1:p.Thr139=
XM_011509293.1:c.428-1659A>C	XP_011507595.1:n.428-1659A>C
NM_000569.7:c.735A>C	NP_000560.6:p.Thr245=
NM_001127592.2:c.732A>C	NP_001121064.2:p.Thr244=
NM_001329120.1:c.420A>C	NP_001316049.1:p.Thr140=
NM_001329122.1:c.635-1659A>C	NP_001316051.1:n.635-1659A>C
XM_024454064.1:c.417A>C	XP_024309832.1:p.Thr139=
NM_001127595.2:c.420A>C	NP_001121067.1:p.Thr140=
NM_001127596.2:c.417A>C	NP_001121068.1:p.Thr139=
NM_000569.8:c.420A>C MANE Select	NP_000560.7:p.Thr140=
NM_001329120.2:c.420A>C	NP_001316049.1:p.Thr140=
NM_001386450.1:c.417A>C	NP_001373379.1:p.Thr139=