Canonical Allele Identifier: CA1221566212

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660007757

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437437dup , CM000663.2:g.218437437dup	GRCh38
NC_000001.10:g.218610779dup , CM000663.1:g.218610779dup	GRCh37
NC_000001.9:g.216677402dup	NCBI36
NG_027721.1:g.97104dup
NG_027721.2:g.97104dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1027dup MANE Select	ENSP00000355897.4:p.Ala343GlyfsTer26
ENST00000366929.4:c.1111dup	ENSP00000355896.4:p.Ala371GlyfsTer26
ENST00000366930.8:c.1027dup	ENSP00000355897.4:p.Ala343GlyfsTer26
ENST00000479322.1:n.511dup
NM_001135599.2:c.1111dup	NP_001129071.1:p.Ala371GlyfsTer26
NM_003238.3:c.1027dup	NP_003229.1:p.Ala343GlyfsTer26
NM_001135599.3:c.1111dup	NP_001129071.1:p.Ala371GlyfsTer26
NM_003238.4:c.1027dup	NP_003229.1:p.Ala343GlyfsTer26
NR_138148.1:n.2330dup
NR_138149.1:n.2414dup
NM_003238.5:c.1027dup	NP_003229.1:p.Ala343GlyfsTer26
NM_003238.6:c.1027dup MANE Select	NP_003229.1:p.Ala343GlyfsTer26
NM_001135599.4:c.1111dup	NP_001129071.1:p.Ala371GlyfsTer26
NR_138148.2:n.2278dup
NR_138149.2:n.2362dup