Canonical Allele Identifier: CA2959481464
Community Standard Title: NM_003238.6(TGFB2):c.*34del
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441396del , CM000663.2:g.218441396del GRCh38
NC_000001.10:g.218614738del , CM000663.1:g.218614738del GRCh37
NC_000001.9:g.216681361del NCBI36
NG_027721.1:g.101063del
NG_027721.2:g.101063del

Transcript Alleles

HGVS Amino-acid Change
NM_003238.6:c.*34del MANE Select NP_003229.1:n.*34del
ENST00000366930.9:c.*34del MANE Select ENSP00000355897.4:n.*34del
NM_001135599.2:c.*34del NP_001129071.1:n.*34del
NM_001135599.3:c.*34del NP_001129071.1:n.*34del
NM_001135599.4:c.*34del NP_001129071.1:n.*34del
NM_003238.3:c.*34del NP_003229.1:n.*34del
NM_003238.4:c.*34del NP_003229.1:n.*34del
NM_003238.5:c.*34del NP_003229.1:n.*34del
NR_138148.1:n.2582del
NR_138148.2:n.2530del
NR_138149.1:n.2666del
NR_138149.2:n.2614del
ENST00000366929.4:c.*34del ENSP00000355896.4:n.*34del
ENST00000366930.8:c.*34del ENSP00000355897.4:n.*34del
ENST00000479322.1:n.763del