Canonical Allele Identifier: CA410117733

Gene: IFNGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33426973A>T , CM000683.2:g.33426973A>T	GRCh38
NC_000021.8:g.34799280A>T , CM000683.1:g.34799280A>T	GRCh37
NC_000021.7:g.33721150A>T	NCBI36
NG_007570.2:g.46982A>T , LRG_67:g.46982A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005534.4:c.502A>T MANE Select	NP_005525.2:p.Thr168Ser
ENST00000290219.11:c.502A>T MANE Select	ENSP00000290219.5:p.Thr168Ser
NM_001329128.1:c.559A>T	NP_001316057.1:p.Thr187Ser
NM_001329128.2:c.559A>T	NP_001316057.1:p.Thr187Ser
NM_005534.3:c.502A>T , LRG_67t1:c.502A>T	NP_005525.2:p.Thr168Ser
ENST00000290219.10:c.502A>T	ENSP00000290219.5:p.Thr168Ser
ENST00000381995.5:c.559A>T	ENSP00000371425.1:p.Thr187Ser
ENST00000405436.5:c.265A>T	ENSP00000385044.1:p.Thr89Ser
ENST00000439213.5:c.*477A>T	ENSP00000407541.1:n.*477A>T
ENST00000545369.2:c.*255A>T	ENSP00000442735.2:n.*255A>T
ENST00000696724.1:c.493A>T	ENSP00000512835.1:p.Thr165Ser
XM_005260969.2:c.559A>T	XP_005261026.1:p.Thr187Ser
XM_011529553.1:c.577A>T	XP_011527855.1:p.Thr193Ser
XM_011529554.1:c.508A>T	XP_011527856.1:p.Thr170Ser
XM_011529554.2:c.508A>T	XP_011527856.1:p.Thr170Ser