Canonical Allele Identifier: CA343367433
Gene: FCGR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544751A>T , CM000663.2:g.161544751A>T GRCh38
NC_000001.10:g.161514541A>T , CM000663.1:g.161514541A>T GRCh37
NC_000001.9:g.159781165A>T NCBI36
NG_009066.1:g.10873T>A , LRG_60:g.10873T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367967.8:c.527T>A ENSP00000356944.3:p.Phe176Tyr
ENST00000426740.8:c.524T>A ENSP00000410180.3:p.Phe175Tyr
ENST00000436743.7:c.527T>A ENSP00000416607.1:p.Phe176Tyr
ENST00000699395.1:c.527T>A ENSP00000514356.1:p.Phe176Tyr
ENST00000699396.1:c.527T>A ENSP00000514357.1:p.Phe176Tyr
ENST00000699397.1:c.527T>A ENSP00000514358.1:p.Phe176Tyr
ENST00000699398.1:c.527T>A ENSP00000514359.1:p.Phe176Tyr
ENST00000699399.1:c.476T>A ENSP00000514360.1:p.Phe159Tyr
ENST00000699400.1:c.524T>A ENSP00000514361.1:p.Phe175Tyr
ENST00000699401.1:c.527T>A ENSP00000514362.1:p.Phe176Tyr
ENST00000426740.7:c.524T>A ENSP00000410180.3:p.Phe175Tyr
ENST00000436743.6:c.527T>A ENSP00000416607.1:p.Phe176Tyr
ENST00000443193.6:c.527T>A MANE Select ENSP00000392047.2:p.Phe176Tyr
ENST00000367967.7:c.527T>A ENSP00000356944.3:p.Phe176Tyr
ENST00000367969.7:c.635T>A ENSP00000356946.3:p.Phe212Tyr
ENST00000426740.5:c.577T>A
ENST00000436743.5:c.527T>A ENSP00000416607.1:p.Phe176Tyr
ENST00000443193.5:c.527T>A ENSP00000392047.2:p.Phe176Tyr
NM_000569.6:c.635T>A NP_000560.5:p.Phe212Tyr
NM_001127592.1:c.632T>A NP_001121064.1:p.Phe211Tyr
NM_001127593.1:c.527T>A , LRG_60t1:c.527T>A NP_001121065.1:p.Phe176Tyr
NM_001127595.1:c.527T>A NP_001121067.1:p.Phe176Tyr
NM_001127596.1:c.524T>A NP_001121068.1:p.Phe175Tyr
XM_011509293.1:c.428-1552T>A XP_011507595.1:n.428-1552T>A
NM_000569.7:c.842T>A NP_000560.6:p.Phe281Tyr
NM_001127592.2:c.839T>A NP_001121064.2:p.Phe280Tyr
NM_001329120.1:c.527T>A NP_001316049.1:p.Phe176Tyr
NM_001329122.1:c.635-1552T>A NP_001316051.1:n.635-1552T>A
XM_024454064.1:c.524T>A XP_024309832.1:p.Phe175Tyr
NM_001127595.2:c.527T>A NP_001121067.1:p.Phe176Tyr
NM_001127596.2:c.524T>A NP_001121068.1:p.Phe175Tyr
NM_000569.8:c.527T>A MANE Select NP_000560.7:p.Phe176Tyr
NM_001329120.2:c.527T>A NP_001316049.1:p.Phe176Tyr
NM_001386450.1:c.524T>A NP_001373379.1:p.Phe175Tyr