Canonical Allele Identifier: CA1140886768

Gene: FCGR1A H2BC18

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149784224C= , CM000663.2:g.149784224C=	GRCh38
NC_000001.10:g.149755780C= , CM000663.1:g.149755780C=	GRCh37
NC_000001.9:g.148022404C=	NCBI36
NG_007578.1:g.6493C= , LRG_59:g.6493C=
NG_033089.1:g.33149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369168.5:c.274C= (FCGR1A) MANE Select	ENSP00000358165.4:p.Arg92=
ENST00000369168.4:c.274C= (FCGR1A)	ENSP00000358165.4:p.Arg92=
ENST00000420462.1:n.76-964G= (H2BC18)
ENST00000444948.5:c.31+1450C= (FCGR1A)	ENSP00000394279.1:n.31+1450C=
ENST00000545683.1:c.378-964G= (H2BC18)	ENSP00000445831.1:n.378-964G=
NM_000566.3:c.274C= , LRG_59t1:c.274C= (FCGR1A)	NP_000557.1:p.Arg92=
NM_001161334.1:c.378-964G= (H2BC18)	NP_001154806.1:n.378-964G=
XM_005244957.2:c.277C= (FCGR1A)	XP_005245014.1:p.Arg93=
XM_005244958.3:c.31+1450C= (FCGR1A)	XP_005245015.1:n.31+1450C=
XM_006711337.2:c.377+27723G= (H2BC18)	XP_006711400.1:n.377+27723G=
XM_005244957.3:c.277C= (FCGR1A)	XP_005245014.1:p.Arg93=
XM_005244958.5:c.31+1450C= (FCGR1A)	XP_005245015.1:n.31+1450C=
NM_000566.4:c.274C= (FCGR1A) MANE Select	NP_000557.1:p.Arg92=
NM_001161334.2:c.378-964G= (H2BC18)	NP_001154806.1:n.378-964G=
NM_001378804.1:c.277C= (FCGR1A)	NP_001365733.1:p.Arg93=
NM_001378805.1:c.253C= (FCGR1A)	NP_001365734.1:p.Arg85=
NM_001378806.1:c.274C= (FCGR1A)	NP_001365735.1:p.Arg92=
NM_001378807.1:c.205C= (FCGR1A)	NP_001365736.1:p.Arg69=
NM_001378808.1:c.274C= (FCGR1A)	NP_001365737.1:p.Arg92=
NM_001378809.1:c.52+1034C= (FCGR1A)	NP_001365738.1:n.52+1034C=
NM_001378810.1:c.31+1450C= (FCGR1A)	NP_001365739.1:n.31+1450C=
NM_001378811.1:c.31+1450C= (FCGR1A)	NP_001365740.1:n.31+1450C=
NR_166121.1:n.324C= (FCGR1A)
NR_166122.1:n.324C= (FCGR1A)
NR_166123.1:n.324C= (FCGR1A)