Canonical Allele Identifier: CA1202785221
Gene: FCGR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544744A= , CM000663.2:g.161544744A= GRCh38
NC_000001.10:g.161514534A= , CM000663.1:g.161514534A= GRCh37
NC_000001.9:g.159781158A= NCBI36
NG_009066.1:g.10880T= , LRG_60:g.10880T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367967.8:c.534T= ENSP00000356944.3:p.Ser178=
ENST00000426740.8:c.531T= ENSP00000410180.3:p.Ser177=
ENST00000436743.7:c.534T= ENSP00000416607.1:p.Ser178=
ENST00000699395.1:c.534T= ENSP00000514356.1:p.Ser178=
ENST00000699396.1:c.534T= ENSP00000514357.1:p.Ser178=
ENST00000699397.1:c.534T= ENSP00000514358.1:p.Ser178=
ENST00000699398.1:c.534T= ENSP00000514359.1:p.Ser178=
ENST00000699399.1:c.483T= ENSP00000514360.1:p.Ser161=
ENST00000699400.1:c.531T= ENSP00000514361.1:p.Ser177=
ENST00000699401.1:c.534T= ENSP00000514362.1:p.Ser178=
ENST00000426740.7:c.531T= ENSP00000410180.3:p.Ser177=
ENST00000436743.6:c.534T= ENSP00000416607.1:p.Ser178=
ENST00000443193.6:c.534T= MANE Select ENSP00000392047.2:p.Ser178=
ENST00000367967.7:c.534T= ENSP00000356944.3:p.Ser178=
ENST00000367969.7:c.642T= ENSP00000356946.3:p.Ser214=
ENST00000426740.5:c.584T=
ENST00000436743.5:c.534T= ENSP00000416607.1:p.Ser178=
ENST00000443193.5:c.534T= ENSP00000392047.2:p.Ser178=
NM_000569.6:c.642T= NP_000560.5:p.Ser214=
NM_001127592.1:c.639T= NP_001121064.1:p.Ser213=
NM_001127593.1:c.534T= , LRG_60t1:c.534T= NP_001121065.1:p.Ser178=
NM_001127595.1:c.534T= NP_001121067.1:p.Ser178=
NM_001127596.1:c.531T= NP_001121068.1:p.Ser177=
XM_011509293.1:c.428-1545T= XP_011507595.1:n.428-1545T=
NM_000569.7:c.849T= NP_000560.6:p.Ser283=
NM_001127592.2:c.846T= NP_001121064.2:p.Ser282=
NM_001329120.1:c.534T= NP_001316049.1:p.Ser178=
NM_001329122.1:c.635-1545T= NP_001316051.1:n.635-1545T=
XM_024454064.1:c.531T= XP_024309832.1:p.Ser177=
NM_001127595.2:c.534T= NP_001121067.1:p.Ser178=
NM_001127596.2:c.531T= NP_001121068.1:p.Ser177=
NM_000569.8:c.534T= MANE Select NP_000560.7:p.Ser178=
NM_001329120.2:c.534T= NP_001316049.1:p.Ser178=
NM_001386450.1:c.531T= NP_001373379.1:p.Ser177=