Canonical Allele Identifier: CA2654302784

Gene: IFNGR2 TMEM50B

Linked Data

• gnomAD v4: 21-33437293-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33437294del , CM000683.2:g.33437294del	GRCh38
NC_000021.8:g.34809601del , CM000683.1:g.34809601del	GRCh37
NC_000021.7:g.33731471del	NCBI36
NG_007570.2:g.57303del , LRG_67:g.57303del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696724.1:c.1337del (IFNGR2)	ENSP00000512835.1:n.1337del
ENST00000290219.11:c.*332del (IFNGR2) MANE Select	ENSP00000290219.5:n.*332del
ENST00000290219.10:c.*332del (IFNGR2)	ENSP00000290219.5:n.*332del
ENST00000381995.5:c.*332del (IFNGR2)	ENSP00000371425.1:n.*332del
ENST00000405436.5:c.*332del (IFNGR2)	ENSP00000385044.1:n.*332del
ENST00000420455.5:c.*2120+1920del (TMEM50B)	ENSP00000397773.1:n.*2120+1920del
ENST00000421802.1:c.176+4423del (IFNGR2)
ENST00000468874.2:n.616-302del (TMEM50B)
ENST00000470682.5:n.359+1920del (TMEM50B)
ENST00000484377.5:n.268-302del (TMEM50B)
NM_005534.3:c.*332del , LRG_67t1:c.*332del (IFNGR2)	NP_005525.2:n.*332del
NR_040016.1:n.2810+1920del (TMEM50B)
XM_005260969.2:c.*332del (IFNGR2)	XP_005261026.1:n.*332del
XM_011529553.1:c.*332del (IFNGR2)	XP_011527855.1:n.*332del
XM_011529554.1:c.*332del (IFNGR2)	XP_011527856.1:n.*332del
XM_011529746.1:c.*2121-302del (TMEM50B)	XP_011528048.1:n.*2121-302del
NM_001329128.1:c.*332del (IFNGR2)	NP_001316057.1:n.*332del
XM_011529554.2:c.*332del (IFNGR2)	XP_011527856.1:n.*332del
XM_011529746.2:c.*2121-302del (TMEM50B)	XP_011528048.1:n.*2121-302del
NM_001329128.2:c.*332del (IFNGR2)	NP_001316057.1:n.*332del
NM_005534.4:c.*332del (IFNGR2) MANE Select	NP_005525.2:n.*332del
NR_040016.2:n.2775+1920del (TMEM50B)