Canonical Allele Identifier: CA2650532593

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441156-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441160del , CM000663.2:g.218441160del	GRCh38
NC_000001.10:g.218614502del , CM000663.1:g.218614502del	GRCh37
NC_000001.9:g.216681125del	NCBI36
NG_027721.1:g.100827del
NG_027721.2:g.100827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1087-44del MANE Select	ENSP00000355897.4:n.1087-44del
ENST00000366929.4:c.1171-44del	ENSP00000355896.4:n.1171-44del
ENST00000366930.8:c.1087-44del	ENSP00000355897.4:n.1087-44del
ENST00000479322.1:n.571-44del
NM_001135599.2:c.1171-44del	NP_001129071.1:n.1171-44del
NM_003238.3:c.1087-44del	NP_003229.1:n.1087-44del
NM_001135599.3:c.1171-44del	NP_001129071.1:n.1171-44del
NM_003238.4:c.1087-44del	NP_003229.1:n.1087-44del
NR_138148.1:n.2390-44del
NR_138149.1:n.2474-44del
NM_003238.5:c.1087-44del	NP_003229.1:n.1087-44del
NM_003238.6:c.1087-44del MANE Select	NP_003229.1:n.1087-44del
NM_001135599.4:c.1171-44del	NP_001129071.1:n.1171-44del
NR_138148.2:n.2338-44del
NR_138149.2:n.2422-44del