Canonical Allele Identifier: CA343367444
Gene: FCGR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544755G>C , CM000663.2:g.161544755G>C GRCh38
NC_000001.10:g.161514545G>C , CM000663.1:g.161514545G>C GRCh37
NC_000001.9:g.159781169G>C NCBI36
NG_009066.1:g.10869C>G , LRG_60:g.10869C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367967.8:c.523C>G ENSP00000356944.3:p.Leu175Val
ENST00000426740.8:c.520C>G ENSP00000410180.3:p.Leu174Val
ENST00000436743.7:c.523C>G ENSP00000416607.1:p.Leu175Val
ENST00000699395.1:c.523C>G ENSP00000514356.1:p.Leu175Val
ENST00000699396.1:c.523C>G ENSP00000514357.1:p.Leu175Val
ENST00000699397.1:c.523C>G ENSP00000514358.1:p.Leu175Val
ENST00000699398.1:c.523C>G ENSP00000514359.1:p.Leu175Val
ENST00000699399.1:c.472C>G ENSP00000514360.1:p.Leu158Val
ENST00000699400.1:c.520C>G ENSP00000514361.1:p.Leu174Val
ENST00000699401.1:c.523C>G ENSP00000514362.1:p.Leu175Val
ENST00000426740.7:c.520C>G ENSP00000410180.3:p.Leu174Val
ENST00000436743.6:c.523C>G ENSP00000416607.1:p.Leu175Val
ENST00000443193.6:c.523C>G MANE Select ENSP00000392047.2:p.Leu175Val
ENST00000367967.7:c.523C>G ENSP00000356944.3:p.Leu175Val
ENST00000367969.7:c.631C>G ENSP00000356946.3:p.Leu211Val
ENST00000426740.5:c.573C>G
ENST00000436743.5:c.523C>G ENSP00000416607.1:p.Leu175Val
ENST00000443193.5:c.523C>G ENSP00000392047.2:p.Leu175Val
NM_000569.6:c.631C>G NP_000560.5:p.Leu211Val
NM_001127592.1:c.628C>G NP_001121064.1:p.Leu210Val
NM_001127593.1:c.523C>G , LRG_60t1:c.523C>G NP_001121065.1:p.Leu175Val
NM_001127595.1:c.523C>G NP_001121067.1:p.Leu175Val
NM_001127596.1:c.520C>G NP_001121068.1:p.Leu174Val
XM_011509293.1:c.428-1556C>G XP_011507595.1:n.428-1556C>G
NM_000569.7:c.838C>G NP_000560.6:p.Leu280Val
NM_001127592.2:c.835C>G NP_001121064.2:p.Leu279Val
NM_001329120.1:c.523C>G NP_001316049.1:p.Leu175Val
NM_001329122.1:c.635-1556C>G NP_001316051.1:n.635-1556C>G
XM_024454064.1:c.520C>G XP_024309832.1:p.Leu174Val
NM_001127595.2:c.523C>G NP_001121067.1:p.Leu175Val
NM_001127596.2:c.520C>G NP_001121068.1:p.Leu174Val
NM_000569.8:c.523C>G MANE Select NP_000560.7:p.Leu175Val
NM_001329120.2:c.523C>G NP_001316049.1:p.Leu175Val
NM_001386450.1:c.520C>G NP_001373379.1:p.Leu174Val