Canonical Allele Identifier: CA1221528604

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346690_218346691delinsCT , CM000663.2:g.218346690_218346691delinsCT	GRCh38
NC_000001.10:g.218520032_218520033delinsCT , CM000663.1:g.218520032_218520033delinsCT	GRCh37
NC_000001.9:g.216586655_216586656delinsCT	NCBI36
NG_027721.1:g.6357_6358delinsCT
NG_027721.2:g.6357_6358delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-12_-11delinsCT MANE Select	ENSP00000355897.4:n.-12_-11delinsCT
ENST00000366929.4:c.-12_-11delinsCT	ENSP00000355896.4:n.-12_-11delinsCT
ENST00000366930.8:c.-12_-11delinsCT	ENSP00000355897.4:n.-12_-11delinsCT
NM_001135599.2:c.-12_-11delinsCT	NP_001129071.1:n.-12_-11delinsCT
NM_003238.3:c.-12_-11delinsCT	NP_003229.1:n.-12_-11delinsCT
NM_001135599.3:c.-12_-11delinsCT	NP_001129071.1:n.-12_-11delinsCT
NM_003238.4:c.-12_-11delinsCT	NP_003229.1:n.-12_-11delinsCT
NR_138148.1:n.1407_1408delinsCT
NR_138149.1:n.1407_1408delinsCT
NM_003238.5:c.-12_-11delinsCT	NP_003229.1:n.-12_-11delinsCT
NM_003238.6:c.-12_-11delinsCT MANE Select	NP_003229.1:n.-12_-11delinsCT
NM_001135599.4:c.-12_-11delinsCT	NP_001129071.1:n.-12_-11delinsCT
NR_138148.2:n.1355_1356delinsCT
NR_138149.2:n.1355_1356delinsCT