Canonical Allele Identifier: CA1211373

Gene: FCGR3A

Linked Data

• dbSNP Id: rs773612051
• ExAC: 1:161514496 G / T
• gnomAD v2: 1-161514496-G-T
• gnomAD v4: 1-161544706-G-T
• MyVariant Identifiers: chr1:g.161514496G>T (hg19) ; chr1:g.161544706G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544706G>T , CM000663.2:g.161544706G>T	GRCh38
NC_000001.10:g.161514496G>T , CM000663.1:g.161514496G>T	GRCh37
NC_000001.9:g.159781120G>T	NCBI36
NG_009066.1:g.10918C>A , LRG_60:g.10918C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367967.8:c.572C>A	ENSP00000356944.3:p.Thr191Asn
ENST00000426740.8:c.569C>A	ENSP00000410180.3:p.Thr190Asn
ENST00000436743.7:c.572C>A	ENSP00000416607.1:p.Thr191Asn
ENST00000699395.1:c.572C>A	ENSP00000514356.1:p.Thr191Asn
ENST00000699396.1:c.572C>A	ENSP00000514357.1:p.Thr191Asn
ENST00000699397.1:c.572C>A	ENSP00000514358.1:p.Thr191Asn
ENST00000699398.1:c.572C>A	ENSP00000514359.1:p.Thr191Asn
ENST00000699399.1:c.521C>A	ENSP00000514360.1:p.Thr174Asn
ENST00000699400.1:c.569C>A	ENSP00000514361.1:p.Thr190Asn
ENST00000699401.1:c.572C>A	ENSP00000514362.1:p.Thr191Asn
ENST00000426740.7:c.569C>A	ENSP00000410180.3:p.Thr190Asn
ENST00000436743.6:c.572C>A	ENSP00000416607.1:p.Thr191Asn
ENST00000443193.6:c.572C>A MANE Select	ENSP00000392047.2:p.Thr191Asn
ENST00000367967.7:c.572C>A	ENSP00000356944.3:p.Thr191Asn
ENST00000367969.7:c.680C>A	ENSP00000356946.3:p.Thr227Asn
ENST00000426740.5:c.622C>A
ENST00000436743.5:c.572C>A	ENSP00000416607.1:p.Thr191Asn
ENST00000443193.5:c.572C>A	ENSP00000392047.2:p.Thr191Asn
NM_000569.6:c.680C>A	NP_000560.5:p.Thr227Asn
NM_001127592.1:c.677C>A	NP_001121064.1:p.Thr226Asn
NM_001127593.1:c.572C>A , LRG_60t1:c.572C>A	NP_001121065.1:p.Thr191Asn
NM_001127595.1:c.572C>A	NP_001121067.1:p.Thr191Asn
NM_001127596.1:c.569C>A	NP_001121068.1:p.Thr190Asn
XM_011509293.1:c.428-1507C>A	XP_011507595.1:n.428-1507C>A
NM_000569.7:c.887C>A	NP_000560.6:p.Thr296Asn
NM_001127592.2:c.884C>A	NP_001121064.2:p.Thr295Asn
NM_001329120.1:c.572C>A	NP_001316049.1:p.Thr191Asn
NM_001329122.1:c.635-1507C>A	NP_001316051.1:n.635-1507C>A
XM_024454064.1:c.569C>A	XP_024309832.1:p.Thr190Asn
NM_001127595.2:c.572C>A	NP_001121067.1:p.Thr191Asn
NM_001127596.2:c.569C>A	NP_001121068.1:p.Thr190Asn
NM_000569.8:c.572C>A MANE Select	NP_000560.7:p.Thr191Asn
NM_001329120.2:c.572C>A	NP_001316049.1:p.Thr191Asn
NM_001386450.1:c.569C>A	NP_001373379.1:p.Thr190Asn