Canonical Allele Identifier: CA916406080

Gene: TGFB2

Linked Data

• dbSNP Id: rs1571820805

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346852dup , CM000663.2:g.218346852dup	GRCh38
NC_000001.10:g.218520194dup , CM000663.1:g.218520194dup	GRCh37
NC_000001.9:g.216586817dup	NCBI36
NG_027721.1:g.6519dup
NG_027721.2:g.6519dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.151dup MANE Select	ENSP00000355897.4:p.Thr51AsnfsTer9
ENST00000366929.4:c.151dup	ENSP00000355896.4:p.Thr51AsnfsTer9
ENST00000366930.8:c.151dup	ENSP00000355897.4:p.Thr51AsnfsTer9
NM_001135599.2:c.151dup	NP_001129071.1:p.Thr51AsnfsTer9
NM_003238.3:c.151dup	NP_003229.1:p.Thr51AsnfsTer9
NM_001135599.3:c.151dup	NP_001129071.1:p.Thr51AsnfsTer9
NM_003238.4:c.151dup	NP_003229.1:p.Thr51AsnfsTer9
NR_138148.1:n.1569dup
NR_138149.1:n.1569dup
NM_003238.5:c.151dup	NP_003229.1:p.Thr51AsnfsTer9
NM_003238.6:c.151dup MANE Select	NP_003229.1:p.Thr51AsnfsTer9
NM_001135599.4:c.151dup	NP_001129071.1:p.Thr51AsnfsTer9
NR_138148.2:n.1517dup
NR_138149.2:n.1517dup