Canonical Allele Identifier: CA1211385
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2212560
ClinVar RCV Id: RCV002677455
dbSNP Id: rs749893099

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161544763C>A , CM000663.2:g.161544763C>A GRCh38
NC_000001.10:g.161514553C>A , CM000663.1:g.161514553C>A GRCh37
NC_000001.9:g.159781177C>A NCBI36
NG_009066.1:g.10861G>T , LRG_60:g.10861G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367967.8:c.515G>T ENSP00000356944.3:p.Cys172Phe
ENST00000426740.8:c.512G>T ENSP00000410180.3:p.Cys171Phe
ENST00000436743.7:c.515G>T ENSP00000416607.1:p.Cys172Phe
ENST00000699395.1:c.515G>T ENSP00000514356.1:p.Cys172Phe
ENST00000699396.1:c.515G>T ENSP00000514357.1:p.Cys172Phe
ENST00000699397.1:c.515G>T ENSP00000514358.1:p.Cys172Phe
ENST00000699398.1:c.515G>T ENSP00000514359.1:p.Cys172Phe
ENST00000699399.1:c.464G>T ENSP00000514360.1:p.Cys155Phe
ENST00000699400.1:c.512G>T ENSP00000514361.1:p.Cys171Phe
ENST00000699401.1:c.515G>T ENSP00000514362.1:p.Cys172Phe
ENST00000426740.7:c.512G>T ENSP00000410180.3:p.Cys171Phe
ENST00000436743.6:c.515G>T ENSP00000416607.1:p.Cys172Phe
ENST00000443193.6:c.515G>T MANE Select ENSP00000392047.2:p.Cys172Phe
ENST00000367967.7:c.515G>T ENSP00000356944.3:p.Cys172Phe
ENST00000367969.7:c.623G>T ENSP00000356946.3:p.Cys208Phe
ENST00000426740.5:c.565G>T
ENST00000436743.5:c.515G>T ENSP00000416607.1:p.Cys172Phe
ENST00000443193.5:c.515G>T ENSP00000392047.2:p.Cys172Phe
NM_000569.6:c.623G>T NP_000560.5:p.Cys208Phe
NM_001127592.1:c.620G>T NP_001121064.1:p.Cys207Phe
NM_001127593.1:c.515G>T , LRG_60t1:c.515G>T NP_001121065.1:p.Cys172Phe
NM_001127595.1:c.515G>T NP_001121067.1:p.Cys172Phe
NM_001127596.1:c.512G>T NP_001121068.1:p.Cys171Phe
XM_011509293.1:c.428-1564G>T XP_011507595.1:n.428-1564G>T
NM_000569.7:c.830G>T NP_000560.6:p.Cys277Phe
NM_001127592.2:c.827G>T NP_001121064.2:p.Cys276Phe
NM_001329120.1:c.515G>T NP_001316049.1:p.Cys172Phe
NM_001329122.1:c.635-1564G>T NP_001316051.1:n.635-1564G>T
XM_024454064.1:c.512G>T XP_024309832.1:p.Cys171Phe
NM_001127595.2:c.515G>T NP_001121067.1:p.Cys172Phe
NM_001127596.2:c.512G>T NP_001121068.1:p.Cys171Phe
NM_000569.8:c.515G>T MANE Select NP_000560.7:p.Cys172Phe
NM_001329120.2:c.515G>T NP_001316049.1:p.Cys172Phe
NM_001386450.1:c.512G>T NP_001373379.1:p.Cys171Phe