Canonical Allele Identifier: CA645531401
Gene: TGFB2 HGNC NCBI

Linked Data

COSMIC: COSM4733359 COSM4733360
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346895del , CM000663.2:g.218346895del GRCh38
NC_000001.10:g.218520237del , CM000663.1:g.218520237del GRCh37
NC_000001.9:g.216586860del NCBI36
NG_027721.1:g.6562del
NG_027721.2:g.6562del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.194del MANE Select ENSP00000355897.4:p.Pro65ArgfsTer3
ENST00000366929.4:c.194del ENSP00000355896.4:p.Pro65ArgfsTer3
ENST00000366930.8:c.194del ENSP00000355897.4:p.Pro65ArgfsTer3
NM_001135599.2:c.194del NP_001129071.1:p.Pro65ArgfsTer3
NM_003238.3:c.194del NP_003229.1:p.Pro65ArgfsTer3
NM_001135599.3:c.194del NP_001129071.1:p.Pro65ArgfsTer3
NM_003238.4:c.194del NP_003229.1:p.Pro65ArgfsTer3
NR_138148.1:n.1612del
NR_138149.1:n.1612del
NM_003238.5:c.194del NP_003229.1:p.Pro65ArgfsTer3
NM_003238.6:c.194del MANE Select NP_003229.1:p.Pro65ArgfsTer3
NM_001135599.4:c.194del NP_001129071.1:p.Pro65ArgfsTer3
NR_138148.2:n.1560del
NR_138149.2:n.1560del
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