Canonical Allele Identifier: CA2650532766

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441579-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441580del , CM000663.2:g.218441580del	GRCh38
NC_000001.10:g.218614922del , CM000663.1:g.218614922del	GRCh37
NC_000001.9:g.216681545del	NCBI36
NG_027721.1:g.101247del
NG_027721.2:g.101247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*218del MANE Select	ENSP00000355897.4:n.*218del
ENST00000366929.4:c.*218del	ENSP00000355896.4:n.*218del
ENST00000366930.8:c.*218del	ENSP00000355897.4:n.*218del
ENST00000479322.1:n.947del
NM_001135599.2:c.*218del	NP_001129071.1:n.*218del
NM_003238.3:c.*218del	NP_003229.1:n.*218del
NM_001135599.3:c.*218del	NP_001129071.1:n.*218del
NM_003238.4:c.*218del	NP_003229.1:n.*218del
NR_138148.1:n.2766del
NR_138149.1:n.2850del
NM_003238.5:c.*218del	NP_003229.1:n.*218del
NM_003238.6:c.*218del MANE Select	NP_003229.1:n.*218del
NM_001135599.4:c.*218del	NP_001129071.1:n.*218del
NR_138148.2:n.2714del
NR_138149.2:n.2798del