Canonical Allele Identifier: CA343367963

Gene: FCGR3A

Linked Data

• gnomAD v4: 1-161544850-T-G
• MyVariant Identifiers: chr1:g.161514640T>G (hg19) ; chr1:g.161544850T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544850T>G , CM000663.2:g.161544850T>G	GRCh38
NC_000001.10:g.161514640T>G , CM000663.1:g.161514640T>G	GRCh37
NC_000001.9:g.159781264T>G	NCBI36
NG_009066.1:g.10774A>C , LRG_60:g.10774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367967.8:c.428A>C	ENSP00000356944.3:p.Gln143Pro
ENST00000426740.8:c.425A>C	ENSP00000410180.3:p.Gln142Pro
ENST00000436743.7:c.428A>C	ENSP00000416607.1:p.Gln143Pro
ENST00000699395.1:c.428A>C	ENSP00000514356.1:p.Gln143Pro
ENST00000699396.1:c.428A>C	ENSP00000514357.1:p.Gln143Pro
ENST00000699397.1:c.428A>C	ENSP00000514358.1:p.Gln143Pro
ENST00000699398.1:c.428A>C	ENSP00000514359.1:p.Gln143Pro
ENST00000699399.1:c.377A>C	ENSP00000514360.1:p.Gln126Pro
ENST00000699400.1:c.425A>C	ENSP00000514361.1:p.Gln142Pro
ENST00000699401.1:c.428A>C	ENSP00000514362.1:p.Gln143Pro
ENST00000699402.1:c.425A>C	ENSP00000514363.1:p.Gln142Pro
ENST00000426740.7:c.425A>C	ENSP00000410180.3:p.Gln142Pro
ENST00000436743.6:c.428A>C	ENSP00000416607.1:p.Gln143Pro
ENST00000443193.6:c.428A>C MANE Select	ENSP00000392047.2:p.Gln143Pro
ENST00000367967.7:c.428A>C	ENSP00000356944.3:p.Gln143Pro
ENST00000367969.7:c.536A>C	ENSP00000356946.3:p.Gln179Pro
ENST00000426740.5:c.478A>C
ENST00000436743.5:c.428A>C	ENSP00000416607.1:p.Gln143Pro
ENST00000443193.5:c.428A>C	ENSP00000392047.2:p.Gln143Pro
NM_000569.6:c.536A>C	NP_000560.5:p.Gln179Pro
NM_001127592.1:c.533A>C	NP_001121064.1:p.Gln178Pro
NM_001127593.1:c.428A>C , LRG_60t1:c.428A>C	NP_001121065.1:p.Gln143Pro
NM_001127595.1:c.428A>C	NP_001121067.1:p.Gln143Pro
NM_001127596.1:c.425A>C	NP_001121068.1:p.Gln142Pro
XM_011509293.1:c.428-1651A>C	XP_011507595.1:n.428-1651A>C
NM_000569.7:c.743A>C	NP_000560.6:p.Gln248Pro
NM_001127592.2:c.740A>C	NP_001121064.2:p.Gln247Pro
NM_001329120.1:c.428A>C	NP_001316049.1:p.Gln143Pro
NM_001329122.1:c.635-1651A>C	NP_001316051.1:n.635-1651A>C
XM_024454064.1:c.425A>C	XP_024309832.1:p.Gln142Pro
NM_001127595.2:c.428A>C	NP_001121067.1:p.Gln143Pro
NM_001127596.2:c.425A>C	NP_001121068.1:p.Gln142Pro
NM_000569.8:c.428A>C MANE Select	NP_000560.7:p.Gln143Pro
NM_001329120.2:c.428A>C	NP_001316049.1:p.Gln143Pro
NM_001386450.1:c.425A>C	NP_001373379.1:p.Gln142Pro