Canonical Allele Identifier: CA2697554954
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2752143
ClinVar RCV Id: RCV003531778
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346790del , CM000663.2:g.218346790del GRCh38
NC_000001.10:g.218520132del , CM000663.1:g.218520132del GRCh37
NC_000001.9:g.216586755del NCBI36
NG_027721.1:g.6457del
NG_027721.2:g.6457del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.89del MANE Select ENSP00000355897.4:p.Asp30AlafsTer16
ENST00000366929.4:c.89del ENSP00000355896.4:p.Asp30AlafsTer16
ENST00000366930.8:c.89del ENSP00000355897.4:p.Asp30AlafsTer16
NM_001135599.2:c.89del NP_001129071.1:p.Asp30AlafsTer16
NM_003238.3:c.89del NP_003229.1:p.Asp30AlafsTer16
NM_001135599.3:c.89del NP_001129071.1:p.Asp30AlafsTer16
NM_003238.4:c.89del NP_003229.1:p.Asp30AlafsTer16
NR_138148.1:n.1507del
NR_138149.1:n.1507del
NM_003238.5:c.89del NP_003229.1:p.Asp30AlafsTer16
NM_003238.6:c.89del MANE Select NP_003229.1:p.Asp30AlafsTer16
NM_001135599.4:c.89del NP_001129071.1:p.Asp30AlafsTer16
NR_138148.2:n.1455del
NR_138149.2:n.1455del
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