Canonical Allele Identifier: CA2574134781
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441172del , CM000663.2:g.218441172del GRCh38
NC_000001.10:g.218614514del , CM000663.1:g.218614514del GRCh37
NC_000001.9:g.216681137del NCBI36
NG_027721.1:g.100839del
NG_027721.2:g.100839del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.1087-32del MANE Select ENSP00000355897.4:n.1087-32del
ENST00000366929.4:c.1171-32del ENSP00000355896.4:n.1171-32del
ENST00000366930.8:c.1087-32del ENSP00000355897.4:n.1087-32del
ENST00000479322.1:n.571-32del
NM_001135599.2:c.1171-32del NP_001129071.1:n.1171-32del
NM_003238.3:c.1087-32del NP_003229.1:n.1087-32del
NM_001135599.3:c.1171-32del NP_001129071.1:n.1171-32del
NM_003238.4:c.1087-32del NP_003229.1:n.1087-32del
NR_138148.1:n.2390-32del
NR_138149.1:n.2474-32del
NM_003238.5:c.1087-32del NP_003229.1:n.1087-32del
NM_003238.6:c.1087-32del MANE Select NP_003229.1:n.1087-32del
NM_001135599.4:c.1171-32del NP_001129071.1:n.1171-32del
NR_138148.2:n.2338-32del
NR_138149.2:n.2422-32del