Canonical Allele Identifier: CA1221568535
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441602_218441604delinsTGA , CM000663.2:g.218441602_218441604delinsTGA GRCh38
NC_000001.10:g.218614944_218614946delinsTGA , CM000663.1:g.218614944_218614946delinsTGA GRCh37
NC_000001.9:g.216681567_216681569delinsTGA NCBI36
NG_027721.1:g.101269_101271delinsTGA
NG_027721.2:g.101269_101271delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.*240_*242delinsTGA MANE Select ENSP00000355897.4:n.*240_*242delinsTGA
ENST00000366929.4:c.*240_*242delinsTGA ENSP00000355896.4:n.*240_*242delinsTGA
ENST00000366930.8:c.*240_*242delinsTGA ENSP00000355897.4:n.*240_*242delinsTGA
ENST00000479322.1:n.969_971delinsTGA
NM_001135599.2:c.*240_*242delinsTGA NP_001129071.1:n.*240_*242delinsTGA
NM_003238.3:c.*240_*242delinsTGA NP_003229.1:n.*240_*242delinsTGA
NM_001135599.3:c.*240_*242delinsTGA NP_001129071.1:n.*240_*242delinsTGA
NM_003238.4:c.*240_*242delinsTGA NP_003229.1:n.*240_*242delinsTGA
NR_138148.1:n.2788_2790delinsTGA
NR_138149.1:n.2872_2874delinsTGA
NM_003238.5:c.*240_*242delinsTGA NP_003229.1:n.*240_*242delinsTGA
NM_003238.6:c.*240_*242delinsTGA MANE Select NP_003229.1:n.*240_*242delinsTGA
NM_001135599.4:c.*240_*242delinsTGA NP_001129071.1:n.*240_*242delinsTGA
NR_138148.2:n.2736_2738delinsTGA
NR_138149.2:n.2820_2822delinsTGA