Canonical Allele Identifier: CA2844618357

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161542558C>G , CM000663.2:g.161542558C>G	GRCh38
NC_000001.10:g.161512348C>G , CM000663.1:g.161512348C>G	GRCh37
NC_000001.9:g.159778972C>G	NCBI36
NG_009066.1:g.13066G>C , LRG_60:g.13066G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.*454G>C	ENSP00000356944.3:n.*454G>C
ENST00000426740.8:c.*454G>C	ENSP00000410180.3:n.*454G>C
ENST00000436743.7:c.*454G>C	ENSP00000416607.1:n.*454G>C
ENST00000699395.1:c.*454G>C	ENSP00000514356.1:n.*454G>C
ENST00000699396.1:c.*454G>C	ENSP00000514357.1:n.*454G>C
ENST00000699397.1:c.*454G>C	ENSP00000514358.1:n.*454G>C
ENST00000699398.1:c.*1931G>C	ENSP00000514359.1:n.*1931G>C
ENST00000699399.1:c.*454G>C	ENSP00000514360.1:n.*454G>C
ENST00000699400.1:c.*454G>C	ENSP00000514361.1:n.*454G>C
ENST00000699401.1:c.*576G>C	ENSP00000514362.1:n.*576G>C
ENST00000426740.7:c.*454G>C	ENSP00000410180.3:n.*454G>C
ENST00000436743.6:c.*454G>C	ENSP00000416607.1:n.*454G>C
ENST00000443193.6:c.*454G>C MANE Select	ENSP00000392047.2:n.*454G>C
ENST00000367967.7:c.*454G>C	ENSP00000356944.3:n.*454G>C
ENST00000367969.7:c.*454G>C	ENSP00000356946.3:n.*454G>C
ENST00000426740.5:c.1269G>C
ENST00000436743.5:c.*454G>C	ENSP00000416607.1:n.*454G>C
ENST00000443193.5:c.*454G>C	ENSP00000392047.2:n.*454G>C
NM_000569.6:c.*454G>C	NP_000560.5:n.*454G>C
NM_001127592.1:c.*454G>C	NP_001121064.1:n.*454G>C
NM_001127593.1:c.*454G>C , LRG_60t1:c.*454G>C	NP_001121065.1:n.*454G>C
NM_001127595.1:c.*454G>C	NP_001121067.1:n.*454G>C
NM_001127596.1:c.*454G>C	NP_001121068.1:n.*454G>C
XM_011509293.1:c.*454G>C	XP_011507595.1:n.*454G>C
NM_000569.7:c.*454G>C	NP_000560.6:n.*454G>C
NM_001127592.2:c.*454G>C	NP_001121064.2:n.*454G>C
NM_001329120.1:c.*454G>C	NP_001316049.1:n.*454G>C
NM_001329122.1:c.*454G>C	NP_001316051.1:n.*454G>C
XM_024454064.1:c.*454G>C	XP_024309832.1:n.*454G>C
NM_001127595.2:c.*454G>C	NP_001121067.1:n.*454G>C
NM_001127596.2:c.*454G>C	NP_001121068.1:n.*454G>C
NM_000569.8:c.*454G>C MANE Select	NP_000560.7:n.*454G>C
NM_001329120.2:c.*454G>C	NP_001316049.1:n.*454G>C
NM_001386450.1:c.*454G>C	NP_001373379.1:n.*454G>C