Canonical Allele Identifier: CA2650532749

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441570-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441570G>A , CM000663.2:g.218441570G>A	GRCh38
NC_000001.10:g.218614912G>A , CM000663.1:g.218614912G>A	GRCh37
NC_000001.9:g.216681535G>A	NCBI36
NG_027721.1:g.101237G>A
NG_027721.2:g.101237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*208G>A MANE Select	ENSP00000355897.4:n.*208G>A
ENST00000366929.4:c.*208G>A	ENSP00000355896.4:n.*208G>A
ENST00000366930.8:c.*208G>A	ENSP00000355897.4:n.*208G>A
ENST00000479322.1:n.937G>A
NM_001135599.2:c.*208G>A	NP_001129071.1:n.*208G>A
NM_003238.3:c.*208G>A	NP_003229.1:n.*208G>A
NM_001135599.3:c.*208G>A	NP_001129071.1:n.*208G>A
NM_003238.4:c.*208G>A	NP_003229.1:n.*208G>A
NR_138148.1:n.2756G>A
NR_138149.1:n.2840G>A
NM_003238.5:c.*208G>A	NP_003229.1:n.*208G>A
NM_003238.6:c.*208G>A MANE Select	NP_003229.1:n.*208G>A
NM_001135599.4:c.*208G>A	NP_001129071.1:n.*208G>A
NR_138148.2:n.2704G>A
NR_138149.2:n.2788G>A