Canonical Allele Identifier: CA1211488

Gene: FCGR3A

Linked Data

• ClinVar Variation Id: 402856
• ClinVar RCV Id: RCV000455515
• dbSNP Id: rs114535887
• ExAC: 1:161518314 C / T
• gnomAD v2: 1-161518314-C-T
• gnomAD v3: 1-161548524-C-T
• gnomAD v4: 1-161548524-C-T
• MyVariant Identifiers: chr1:g.161518314C>T (hg19) ; chr1:g.161548524C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161548524C>T , CM000663.2:g.161548524C>T	GRCh38
NC_000001.10:g.161518314C>T , CM000663.1:g.161518314C>T	GRCh37
NC_000001.9:g.159784938C>T	NCBI36
NG_009066.1:g.7100G>A , LRG_60:g.7100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.216G>A	ENSP00000356944.3:p.Ser72=
ENST00000426740.8:c.213G>A	ENSP00000410180.3:p.Ser71=
ENST00000436743.7:c.216G>A	ENSP00000416607.1:p.Ser72=
ENST00000442336.2:c.213G>A	ENSP00000396567.2:p.Ser71=
ENST00000699395.1:c.216G>A	ENSP00000514356.1:p.Ser72=
ENST00000699396.1:c.216G>A	ENSP00000514357.1:p.Ser72=
ENST00000699397.1:c.216G>A	ENSP00000514358.1:p.Ser72=
ENST00000699398.1:c.216G>A	ENSP00000514359.1:p.Ser72=
ENST00000699399.1:c.165G>A	ENSP00000514360.1:p.Ser55=
ENST00000699400.1:c.213G>A	ENSP00000514361.1:p.Ser71=
ENST00000699401.1:c.216G>A	ENSP00000514362.1:p.Ser72=
ENST00000699402.1:c.213G>A	ENSP00000514363.1:p.Ser71=
ENST00000699403.1:c.216G>A	ENSP00000514364.1:p.Ser72=
ENST00000699493.1:c.216G>A	ENSP00000514404.1:p.Ser72=
ENST00000426740.7:c.213G>A	ENSP00000410180.3:p.Ser71=
ENST00000436743.6:c.216G>A	ENSP00000416607.1:p.Ser72=
ENST00000443193.6:c.216G>A MANE Select	ENSP00000392047.2:p.Ser72=
ENST00000367967.7:c.216G>A	ENSP00000356944.3:p.Ser72=
ENST00000367969.7:c.324G>A	ENSP00000356946.3:p.Ser108=
ENST00000426740.5:c.266G>A
ENST00000436743.5:c.216G>A	ENSP00000416607.1:p.Ser72=
ENST00000442336.1:c.213G>A	ENSP00000396567.1:p.Ser71=
ENST00000443193.5:c.216G>A	ENSP00000392047.2:p.Ser72=
ENST00000476031.1:n.210G>A
NM_000569.6:c.324G>A	NP_000560.5:p.Ser108=
NM_001127592.1:c.321G>A	NP_001121064.1:p.Ser107=
NM_001127593.1:c.216G>A , LRG_60t1:c.216G>A	NP_001121065.1:p.Ser72=
NM_001127595.1:c.216G>A	NP_001121067.1:p.Ser72=
NM_001127596.1:c.213G>A	NP_001121068.1:p.Ser71=
XM_011509293.1:c.324G>A	XP_011507595.1:p.Ser108=
NM_000569.7:c.531G>A	NP_000560.6:p.Ser177=
NM_001127592.2:c.528G>A	NP_001121064.2:p.Ser176=
NM_001329120.1:c.216G>A	NP_001316049.1:p.Ser72=
NM_001329122.1:c.531G>A	NP_001316051.1:p.Ser177=
XM_024454064.1:c.213G>A	XP_024309832.1:p.Ser71=
NM_001127595.2:c.216G>A	NP_001121067.1:p.Ser72=
NM_001127596.2:c.213G>A	NP_001121068.1:p.Ser71=
NM_000569.8:c.216G>A MANE Select	NP_000560.7:p.Ser72=
NM_001329120.2:c.216G>A	NP_001316049.1:p.Ser72=
NM_001386450.1:c.213G>A	NP_001373379.1:p.Ser71=