Canonical Allele Identifier: CA2747782692

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437382_218437383insAGG , CM000663.2:g.218437382_218437383insAGG	GRCh38
NC_000001.10:g.218610724_218610725insAGG , CM000663.1:g.218610724_218610725insAGG	GRCh37
NC_000001.9:g.216677347_216677348insAGG	NCBI36
NG_027721.1:g.97049_97050insAGG
NG_027721.2:g.97049_97050insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.972_973insAGG MANE Select	ENSP00000355897.4:p.Ile324_Asp325insArg
ENST00000366929.4:c.1056_1057insAGG	ENSP00000355896.4:p.Ile352_Asp353insArg
ENST00000366930.8:c.972_973insAGG	ENSP00000355897.4:p.Ile324_Asp325insArg
ENST00000479322.1:n.456_457insAGG
NM_001135599.2:c.1056_1057insAGG	NP_001129071.1:p.Ile352_Asp353insArg
NM_003238.3:c.972_973insAGG	NP_003229.1:p.Ile324_Asp325insArg
NM_001135599.3:c.1056_1057insAGG	NP_001129071.1:p.Ile352_Asp353insArg
NM_003238.4:c.972_973insAGG	NP_003229.1:p.Ile324_Asp325insArg
NR_138148.1:n.2275_2276insAGG
NR_138149.1:n.2359_2360insAGG
NM_003238.5:c.972_973insAGG	NP_003229.1:p.Ile324_Asp325insArg
NM_003238.6:c.972_973insAGG MANE Select	NP_003229.1:p.Ile324_Asp325insArg
NM_001135599.4:c.1056_1057insAGG	NP_001129071.1:p.Ile352_Asp353insArg
NR_138148.2:n.2223_2224insAGG
NR_138149.2:n.2307_2308insAGG