Canonical Allele Identifier: CA343368520

Gene: FCGR3A

Linked Data

• MyVariant Identifiers: chr1:g.161514745C>T (hg19) ; chr1:g.161544955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544955C>T , CM000663.2:g.161544955C>T	GRCh38
NC_000001.10:g.161514745C>T , CM000663.1:g.161514745C>T	GRCh37
NC_000001.9:g.159781369C>T	NCBI36
NG_009066.1:g.10669G>A , LRG_60:g.10669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.323G>A	ENSP00000356944.3:p.Trp108Ter
ENST00000426740.8:c.320G>A	ENSP00000410180.3:p.Trp107Ter
ENST00000436743.7:c.323G>A	ENSP00000416607.1:p.Trp108Ter
ENST00000442336.2:c.320G>A	ENSP00000396567.2:p.Trp107Ter
ENST00000699395.1:c.323G>A	ENSP00000514356.1:p.Trp108Ter
ENST00000699396.1:c.323G>A	ENSP00000514357.1:p.Trp108Ter
ENST00000699397.1:c.323G>A	ENSP00000514358.1:p.Trp108Ter
ENST00000699398.1:c.323G>A	ENSP00000514359.1:p.Trp108Ter
ENST00000699399.1:c.272G>A	ENSP00000514360.1:p.Trp91Ter
ENST00000699400.1:c.320G>A	ENSP00000514361.1:p.Trp107Ter
ENST00000699401.1:c.323G>A	ENSP00000514362.1:p.Trp108Ter
ENST00000699402.1:c.320G>A	ENSP00000514363.1:p.Trp107Ter
ENST00000699493.1:c.*55G>A	ENSP00000514404.1:n.*55G>A
ENST00000426740.7:c.320G>A	ENSP00000410180.3:p.Trp107Ter
ENST00000436743.6:c.323G>A	ENSP00000416607.1:p.Trp108Ter
ENST00000443193.6:c.323G>A MANE Select	ENSP00000392047.2:p.Trp108Ter
ENST00000367967.7:c.323G>A	ENSP00000356944.3:p.Trp108Ter
ENST00000367969.7:c.431G>A	ENSP00000356946.3:p.Trp144Ter
ENST00000426740.5:c.373G>A
ENST00000436743.5:c.323G>A	ENSP00000416607.1:p.Trp108Ter
ENST00000443193.5:c.323G>A	ENSP00000392047.2:p.Trp108Ter
NM_000569.6:c.431G>A	NP_000560.5:p.Trp144Ter
NM_001127592.1:c.428G>A	NP_001121064.1:p.Trp143Ter
NM_001127593.1:c.323G>A , LRG_60t1:c.323G>A	NP_001121065.1:p.Trp108Ter
NM_001127595.1:c.323G>A	NP_001121067.1:p.Trp108Ter
NM_001127596.1:c.320G>A	NP_001121068.1:p.Trp107Ter
XM_011509293.1:c.428-1756G>A	XP_011507595.1:n.428-1756G>A
NM_000569.7:c.638G>A	NP_000560.6:p.Trp213Ter
NM_001127592.2:c.635G>A	NP_001121064.2:p.Trp212Ter
NM_001329120.1:c.323G>A	NP_001316049.1:p.Trp108Ter
NM_001329122.1:c.635-1756G>A	NP_001316051.1:n.635-1756G>A
XM_024454064.1:c.320G>A	XP_024309832.1:p.Trp107Ter
NM_001127595.2:c.323G>A	NP_001121067.1:p.Trp108Ter
NM_001127596.2:c.320G>A	NP_001121068.1:p.Trp107Ter
NM_000569.8:c.323G>A MANE Select	NP_000560.7:p.Trp108Ter
NM_001329120.2:c.323G>A	NP_001316049.1:p.Trp108Ter
NM_001386450.1:c.320G>A	NP_001373379.1:p.Trp107Ter