Canonical Allele Identifier: CA124361
Gene: FCGR2A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14823
dbSNP Id: rs1801274

User contributed link-outs

CIViC: CA124361

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161509955A>G , CM000663.2:g.161509955A>G GRCh38
NC_000001.10:g.161479745A>G , CM000663.1:g.161479745A>G GRCh37
NC_000001.9:g.159746369A>G NCBI36
NG_012066.1:g.9541A>G
NG_012066.2:g.9541A>G

Transcript Alleles

HGVS Amino-acid change
NM_001136219.1:c.500A>G VV NP_001129691.1:p.His167Arg
NM_021642.3:c.497A>G VV NP_067674.2:p.His166Arg
XM_011509287.1:c.500A>G XP_011507589.1:p.His167Arg
XM_011509288.1:c.497A>G XP_011507590.1:p.His166Arg
XM_011509289.1:c.500A>G XP_011507591.1:p.His167Arg
XM_011509290.1:c.500A>G XP_011507592.1:p.His167Arg
XM_011509291.1:c.500A>G XP_011507593.1:p.His167Arg
XM_011509287.2:c.500A>G XP_011507589.1:p.His167Arg
XM_011509290.2:c.500A>G XP_011507592.1:p.His167Arg
XM_017000663.2:c.497A>G XP_016856152.1:p.His166Arg
XM_017000664.1:c.500A>G XP_016856153.1:p.His167Arg
XM_017000665.1:c.500A>G XP_016856154.1:p.His167Arg
XM_017000666.1:c.500A>G XP_016856155.1:p.His167Arg
XM_017000667.1:c.500A>G XP_016856156.1:p.His167Arg
XM_017000668.2:c.497A>G XP_016856157.1:p.His166Arg
XM_024454040.1:c.83A>G XP_024309808.1:p.His28Arg
XM_024454041.1:c.83A>G XP_024309809.1:p.His28Arg
XR_001737042.1:n.538A>G
ENST00000271450.10:c.500A>G ENSP00000271450.6:p.His167Arg
ENST00000367972.8:c.497A>G ENSP00000356949.4:p.His166Arg
ENST00000467525.5:n.395A>G ENSP00000476495.1:p.His132Arg
ENST00000467654.1:n.519A>G
ENST00000471026.5:n.193A>G
ENST00000483665.6:c.*202A>G ENSP00000440148.1:p.=