Canonical Allele Identifier: CA1148287400
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346655_218346660delinsTTTATT , CM000663.2:g.218346655_218346660delinsTTTATT GRCh38
NC_000001.10:g.218519997_218520002delinsTTTATT , CM000663.1:g.218519997_218520002delinsTTTATT GRCh37
NC_000001.9:g.216586620_216586625delinsTTTATT NCBI36
NG_027721.1:g.6322_6327delinsTTTATT
NG_027721.2:g.6322_6327delinsTTTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-47_-42delinsTTTATT MANE Select ENSP00000355897.4:n.-47_-42delinsTTTATT
ENST00000366929.4:c.-47_-42delinsTTTATT ENSP00000355896.4:n.-47_-42delinsTTTATT
ENST00000366930.8:c.-47_-42delinsTTTATT ENSP00000355897.4:n.-47_-42delinsTTTATT
NM_001135599.2:c.-47_-42delinsTTTATT NP_001129071.1:n.-47_-42delinsTTTATT
NM_003238.3:c.-47_-42delinsTTTATT NP_003229.1:n.-47_-42delinsTTTATT
NM_001135599.3:c.-47_-42delinsTTTATT NP_001129071.1:n.-47_-42delinsTTTATT
NM_003238.4:c.-47_-42delinsTTTATT NP_003229.1:n.-47_-42delinsTTTATT
NR_138148.1:n.1372_1377delinsTTTATT
NR_138149.1:n.1372_1377delinsTTTATT
NM_003238.5:c.-47_-42delinsTTTATT NP_003229.1:n.-47_-42delinsTTTATT
NM_003238.6:c.-47_-42delinsTTTATT MANE Select NP_003229.1:n.-47_-42delinsTTTATT
NM_001135599.4:c.-47_-42delinsTTTATT NP_001129071.1:n.-47_-42delinsTTTATT
NR_138148.2:n.1320_1325delinsTTTATT
NR_138149.2:n.1320_1325delinsTTTATT