Canonical Allele Identifier: CA1221528585
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346654_218346658delinsTTTTA , CM000663.2:g.218346654_218346658delinsTTTTA GRCh38
NC_000001.10:g.218519996_218520000delinsTTTTA , CM000663.1:g.218519996_218520000delinsTTTTA GRCh37
NC_000001.9:g.216586619_216586623delinsTTTTA NCBI36
NG_027721.1:g.6321_6325delinsTTTTA
NG_027721.2:g.6321_6325delinsTTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-48_-44delinsTTTTA MANE Select ENSP00000355897.4:n.-48_-44delinsTTTTA
ENST00000366929.4:c.-48_-44delinsTTTTA ENSP00000355896.4:n.-48_-44delinsTTTTA
ENST00000366930.8:c.-48_-44delinsTTTTA ENSP00000355897.4:n.-48_-44delinsTTTTA
NM_001135599.2:c.-48_-44delinsTTTTA NP_001129071.1:n.-48_-44delinsTTTTA
NM_003238.3:c.-48_-44delinsTTTTA NP_003229.1:n.-48_-44delinsTTTTA
NM_001135599.3:c.-48_-44delinsTTTTA NP_001129071.1:n.-48_-44delinsTTTTA
NM_003238.4:c.-48_-44delinsTTTTA NP_003229.1:n.-48_-44delinsTTTTA
NR_138148.1:n.1371_1375delinsTTTTA
NR_138149.1:n.1371_1375delinsTTTTA
NM_003238.5:c.-48_-44delinsTTTTA NP_003229.1:n.-48_-44delinsTTTTA
NM_003238.6:c.-48_-44delinsTTTTA MANE Select NP_003229.1:n.-48_-44delinsTTTTA
NM_001135599.4:c.-48_-44delinsTTTTA NP_001129071.1:n.-48_-44delinsTTTTA
NR_138148.2:n.1319_1323delinsTTTTA
NR_138149.2:n.1319_1323delinsTTTTA