Canonical Allele Identifier: CA2650532729

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441549-TCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441550_218441552del , CM000663.2:g.218441550_218441552del	GRCh38
NC_000001.10:g.218614892_218614894del , CM000663.1:g.218614892_218614894del	GRCh37
NC_000001.9:g.216681515_216681517del	NCBI36
NG_027721.1:g.101217_101219del
NG_027721.2:g.101217_101219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*188_*190del MANE Select	ENSP00000355897.4:n.*188_*190del
ENST00000366929.4:c.*188_*190del	ENSP00000355896.4:n.*188_*190del
ENST00000366930.8:c.*188_*190del	ENSP00000355897.4:n.*188_*190del
ENST00000479322.1:n.917_919del
NM_001135599.2:c.*188_*190del	NP_001129071.1:n.*188_*190del
NM_003238.3:c.*188_*190del	NP_003229.1:n.*188_*190del
NM_001135599.3:c.*188_*190del	NP_001129071.1:n.*188_*190del
NM_003238.4:c.*188_*190del	NP_003229.1:n.*188_*190del
NR_138148.1:n.2736_2738del
NR_138149.1:n.2820_2822del
NM_003238.5:c.*188_*190del	NP_003229.1:n.*188_*190del
NM_003238.6:c.*188_*190del MANE Select	NP_003229.1:n.*188_*190del
NM_001135599.4:c.*188_*190del	NP_001129071.1:n.*188_*190del
NR_138148.2:n.2684_2686del
NR_138149.2:n.2768_2770del