Canonical Allele Identifier: CA1211499
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 402857
dbSNP Id: rs10127939

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161548543A>C , CM000663.2:g.161548543A>C GRCh38
NC_000001.10:g.161518333A>C , CM000663.1:g.161518333A>C GRCh37
NC_000001.9:g.159784957A>C NCBI36
NG_009066.1:g.7081T>G , LRG_60:g.7081T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367967.8:c.197T>G ENSP00000356944.3:p.Leu66Arg
ENST00000426740.8:c.194T>G ENSP00000410180.3:p.Leu65Arg
ENST00000436743.7:c.197T>G ENSP00000416607.1:p.Leu66Arg
ENST00000442336.2:c.194T>G ENSP00000396567.2:p.Leu65Arg
ENST00000699395.1:c.197T>G ENSP00000514356.1:p.Leu66Arg
ENST00000699396.1:c.197T>G ENSP00000514357.1:p.Leu66Arg
ENST00000699397.1:c.197T>G ENSP00000514358.1:p.Leu66Arg
ENST00000699398.1:c.197T>G ENSP00000514359.1:p.Leu66Arg
ENST00000699399.1:c.146T>G ENSP00000514360.1:p.Leu49Arg
ENST00000699400.1:c.194T>G ENSP00000514361.1:p.Leu65Arg
ENST00000699401.1:c.197T>G ENSP00000514362.1:p.Leu66Arg
ENST00000699402.1:c.194T>G ENSP00000514363.1:p.Leu65Arg
ENST00000699403.1:c.197T>G ENSP00000514364.1:p.Leu66Arg
ENST00000699493.1:c.197T>G ENSP00000514404.1:p.Leu66Arg
ENST00000426740.7:c.194T>G ENSP00000410180.3:p.Leu65Arg
ENST00000436743.6:c.197T>G ENSP00000416607.1:p.Leu66Arg
ENST00000443193.6:c.197T>G MANE Select ENSP00000392047.2:p.Leu66Arg
ENST00000367967.7:c.197T>G ENSP00000356944.3:p.Leu66Arg
ENST00000367969.7:c.305T>G ENSP00000356946.3:p.Leu102Arg
ENST00000426740.5:c.247T>G
ENST00000436743.5:c.197T>G ENSP00000416607.1:p.Leu66Arg
ENST00000442336.1:c.194T>G ENSP00000396567.1:p.Leu65Arg
ENST00000443193.5:c.197T>G ENSP00000392047.2:p.Leu66Arg
ENST00000476031.1:n.191T>G
NM_000569.6:c.305T>G NP_000560.5:p.Leu102Arg
NM_001127592.1:c.302T>G NP_001121064.1:p.Leu101Arg
NM_001127593.1:c.197T>G , LRG_60t1:c.197T>G NP_001121065.1:p.Leu66Arg
NM_001127595.1:c.197T>G NP_001121067.1:p.Leu66Arg
NM_001127596.1:c.194T>G NP_001121068.1:p.Leu65Arg
XM_011509293.1:c.305T>G XP_011507595.1:p.Leu102Arg
NM_000569.7:c.512T>G NP_000560.6:p.Leu171Arg
NM_001127592.2:c.509T>G NP_001121064.2:p.Leu170Arg
NM_001329120.1:c.197T>G NP_001316049.1:p.Leu66Arg
NM_001329122.1:c.512T>G NP_001316051.1:p.Leu171Arg
XM_024454064.1:c.194T>G XP_024309832.1:p.Leu65Arg
NM_001127595.2:c.197T>G NP_001121067.1:p.Leu66Arg
NM_001127596.2:c.194T>G NP_001121068.1:p.Leu65Arg
NM_000569.8:c.197T>G MANE Select NP_000560.7:p.Leu66Arg
NM_001329120.2:c.197T>G NP_001316049.1:p.Leu66Arg
NM_001386450.1:c.194T>G NP_001373379.1:p.Leu65Arg