Canonical Allele Identifier: CA2386670063

Gene: IFNGR2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33424579A>T , CM000683.2:g.33424579A>T	GRCh38
NC_000021.8:g.34796886A>T , CM000683.1:g.34796886A>T	GRCh37
NC_000021.7:g.33718756A>T	NCBI36
NG_007570.2:g.44588A>T , LRG_67:g.44588A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696724.1:c.308-523A>T	ENSP00000512835.1:n.308-523A>T
ENST00000290219.11:c.413-2305A>T MANE Select	ENSP00000290219.5:n.413-2305A>T
ENST00000290219.10:c.413-2305A>T	ENSP00000290219.5:n.413-2305A>T
ENST00000381995.5:c.470-2305A>T	ENSP00000371425.1:n.470-2305A>T
ENST00000405436.5:c.176-2305A>T	ENSP00000385044.1:n.176-2305A>T
ENST00000439213.5:c.*388-2305A>T	ENSP00000407541.1:n.*388-2305A>T
ENST00000545369.2:c.*166-2305A>T	ENSP00000442735.2:n.*166-2305A>T
NM_005534.3:c.413-2305A>T , LRG_67t1:c.413-2305A>T	NP_005525.2:n.413-2305A>T
XM_005260969.2:c.470-2305A>T	XP_005261026.1:n.470-2305A>T
XM_011529553.1:c.488-2305A>T	XP_011527855.1:n.488-2305A>T
XM_011529554.1:c.419-2305A>T	XP_011527856.1:n.419-2305A>T
NM_001329128.1:c.470-2305A>T	NP_001316057.1:n.470-2305A>T
XM_011529554.2:c.419-2305A>T	XP_011527856.1:n.419-2305A>T
NM_001329128.2:c.470-2305A>T	NP_001316057.1:n.470-2305A>T
NM_005534.4:c.413-2305A>T MANE Select	NP_005525.2:n.413-2305A>T