Canonical Allele Identifier: CA410117622

Gene: IFNGR2

Linked Data

• MyVariant Identifiers: chr21:g.34799229G>C (hg19) ; chr21:g.33426922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33426922G>C , CM000683.2:g.33426922G>C	GRCh38
NC_000021.8:g.34799229G>C , CM000683.1:g.34799229G>C	GRCh37
NC_000021.7:g.33721099G>C	NCBI36
NG_007570.2:g.46931G>C , LRG_67:g.46931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696724.1:c.442G>C	ENSP00000512835.1:p.Gly148Arg
ENST00000290219.11:c.451G>C MANE Select	ENSP00000290219.5:p.Gly151Arg
ENST00000290219.10:c.451G>C	ENSP00000290219.5:p.Gly151Arg
ENST00000381995.5:c.508G>C	ENSP00000371425.1:p.Gly170Arg
ENST00000405436.5:c.214G>C	ENSP00000385044.1:p.Gly72Arg
ENST00000439213.5:c.*426G>C	ENSP00000407541.1:n.*426G>C
ENST00000545369.2:c.*204G>C	ENSP00000442735.2:n.*204G>C
NM_005534.3:c.451G>C , LRG_67t1:c.451G>C	NP_005525.2:p.Gly151Arg
XM_005260969.2:c.508G>C	XP_005261026.1:p.Gly170Arg
XM_011529553.1:c.526G>C	XP_011527855.1:p.Gly176Arg
XM_011529554.1:c.457G>C	XP_011527856.1:p.Gly153Arg
NM_001329128.1:c.508G>C	NP_001316057.1:p.Gly170Arg
XM_011529554.2:c.457G>C	XP_011527856.1:p.Gly153Arg
NM_001329128.2:c.508G>C	NP_001316057.1:p.Gly170Arg
NM_005534.4:c.451G>C MANE Select	NP_005525.2:p.Gly151Arg