Canonical Allele Identifier: CA2739275663
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2920683
ClinVar RCV Id: RCV003649154

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346710del , CM000663.2:g.218346710del GRCh38
NC_000001.10:g.218520052del , CM000663.1:g.218520052del GRCh37
NC_000001.9:g.216586675del NCBI36
NG_027721.1:g.6377del
NG_027721.2:g.6377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.9del MANE Select ENSP00000355897.4:p.Cys4ValfsTer3
ENST00000366929.4:c.9del ENSP00000355896.4:p.Cys4ValfsTer3
ENST00000366930.8:c.9del ENSP00000355897.4:p.Cys4ValfsTer3
NM_001135599.2:c.9del NP_001129071.1:p.Cys4ValfsTer3
NM_003238.3:c.9del NP_003229.1:p.Cys4ValfsTer3
NM_001135599.3:c.9del NP_001129071.1:p.Cys4ValfsTer3
NM_003238.4:c.9del NP_003229.1:p.Cys4ValfsTer3
NR_138148.1:n.1427del
NR_138149.1:n.1427del
NM_003238.5:c.9del NP_003229.1:p.Cys4ValfsTer3
NM_003238.6:c.9del MANE Select NP_003229.1:p.Cys4ValfsTer3
NM_001135599.4:c.9del NP_001129071.1:p.Cys4ValfsTer3
NR_138148.2:n.1375del
NR_138149.2:n.1375del