Canonical Allele Identifier: CA1144233579

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437431_218437436delinsTACAAT , CM000663.2:g.218437431_218437436delinsTACAAT	GRCh38
NC_000001.10:g.218610773_218610778delinsTACAAT , CM000663.1:g.218610773_218610778delinsTACAAT	GRCh37
NC_000001.9:g.216677396_216677401delinsTACAAT	NCBI36
NG_027721.1:g.97098_97103delinsTACAAT
NG_027721.2:g.97098_97103delinsTACAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1021_1026delinsTACAAT MANE Select	ENSP00000355897.4:p.Tyr341=
ENST00000366929.4:c.1105_1110delinsTACAAT	ENSP00000355896.4:p.Tyr369=
ENST00000366930.8:c.1021_1026delinsTACAAT	ENSP00000355897.4:p.Tyr341=
ENST00000479322.1:n.505_510delinsTACAAT
NM_001135599.2:c.1105_1110delinsTACAAT	NP_001129071.1:p.Tyr369=
NM_003238.3:c.1021_1026delinsTACAAT	NP_003229.1:p.Tyr341=
NM_001135599.3:c.1105_1110delinsTACAAT	NP_001129071.1:p.Tyr369=
NM_003238.4:c.1021_1026delinsTACAAT	NP_003229.1:p.Tyr341=
NR_138148.1:n.2324_2329delinsTACAAT
NR_138149.1:n.2408_2413delinsTACAAT
NM_003238.5:c.1021_1026delinsTACAAT	NP_003229.1:p.Tyr341=
NM_003238.6:c.1021_1026delinsTACAAT MANE Select	NP_003229.1:p.Tyr341=
NM_001135599.4:c.1105_1110delinsTACAAT	NP_001129071.1:p.Tyr369=
NR_138148.2:n.2272_2277delinsTACAAT
NR_138149.2:n.2356_2361delinsTACAAT