Canonical Allele Identifier: CA2577478432

Gene: IFNGR2

Linked Data

• ClinVar Variation Id: 2068974
• ClinVar RCV Id: RCV002975243
• gnomAD v4: 21-33403623-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33403623C>T , CM000683.2:g.33403623C>T	GRCh38
NC_000021.8:g.34775929C>T , CM000683.1:g.34775929C>T	GRCh37
NC_000021.7:g.33697799C>T	NCBI36
NG_007570.2:g.23631C>T , LRG_67:g.23631C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290219.11:c.73+7C>T MANE Select	ENSP00000290219.5:n.73+7C>T
ENST00000290219.10:c.73+7C>T	ENSP00000290219.5:n.73+7C>T
ENST00000381995.5:c.73+7C>T	ENSP00000371425.1:n.73+7C>T
ENST00000405436.5:c.-217+7C>T	ENSP00000385044.1:n.-217+7C>T
ENST00000439213.5:c.73+7C>T	ENSP00000407541.1:n.73+7C>T
ENST00000545369.2:c.73+7C>T	ENSP00000442735.2:n.73+7C>T
NM_005534.3:c.73+7C>T , LRG_67t1:c.73+7C>T	NP_005525.2:n.73+7C>T
XM_005260969.2:c.73+7C>T	XP_005261026.1:n.73+7C>T
NM_001329128.1:c.73+7C>T	NP_001316057.1:n.73+7C>T
NM_001329128.2:c.73+7C>T	NP_001316057.1:n.73+7C>T
NM_005534.4:c.73+7C>T MANE Select	NP_005525.2:n.73+7C>T