Canonical Allele Identifier: CA1139666835

Gene: IFNGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33403547del , CM000683.2:g.33403547del	GRCh38
NC_000021.8:g.34775853del , CM000683.1:g.34775853del	GRCh37
NC_000021.7:g.33697723del	NCBI36
NG_007570.2:g.23555del , LRG_67:g.23555del

Transcript Alleles

HGVS	Amino-acid Change
NM_005534.4:c.4del MANE Select	NP_005525.2:p.Arg2AspfsTer?
ENST00000290219.11:c.4del MANE Select	ENSP00000290219.5:p.Arg2AspfsTer?
NM_001329128.1:c.4del	NP_001316057.1:p.Arg2AspfsTer26
NM_001329128.2:c.4del	NP_001316057.1:p.Arg2AspfsTer26
NM_005534.3:c.4del , LRG_67t1:c.4del	NP_005525.2:p.Arg2AspfsTer?
ENST00000290219.10:c.4del	ENSP00000290219.5:p.Arg2AspfsTer?
ENST00000381995.5:c.4del	ENSP00000371425.1:p.Arg2AspfsTer26
ENST00000405436.5:c.-286del	ENSP00000385044.1:n.-286del
ENST00000439213.5:c.4del	ENSP00000407541.1:p.Arg2AspfsTer26
ENST00000545369.2:c.4del	ENSP00000442735.2:p.Arg2AspfsTer27
XM_005260969.2:c.4del	XP_005261026.1:p.Arg2AspfsTer26