Canonical Allele Identifier: CA2739275667

Gene: TGFB2

Linked Data

• ClinVar Variation Id: 2899783
• ClinVar RCV Id: RCV003648891

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437369del , CM000663.2:g.218437369del	GRCh38
NC_000001.10:g.218610711del , CM000663.1:g.218610711del	GRCh37
NC_000001.9:g.216677334del	NCBI36
NG_027721.1:g.97036del
NG_027721.2:g.97036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.959del MANE Select	ENSP00000355897.4:p.Arg320LeufsTer11
ENST00000366929.4:c.1043del	ENSP00000355896.4:p.Arg348LeufsTer11
ENST00000366930.8:c.959del	ENSP00000355897.4:p.Arg320LeufsTer11
ENST00000479322.1:n.443del
NM_001135599.2:c.1043del	NP_001129071.1:p.Arg348LeufsTer11
NM_003238.3:c.959del	NP_003229.1:p.Arg320LeufsTer11
NM_001135599.3:c.1043del	NP_001129071.1:p.Arg348LeufsTer11
NM_003238.4:c.959del	NP_003229.1:p.Arg320LeufsTer11
NR_138148.1:n.2262del
NR_138149.1:n.2346del
NM_003238.5:c.959del	NP_003229.1:p.Arg320LeufsTer11
NM_003238.6:c.959del MANE Select	NP_003229.1:p.Arg320LeufsTer11
NM_001135599.4:c.1043del	NP_001129071.1:p.Arg348LeufsTer11
NR_138148.2:n.2210del
NR_138149.2:n.2294del