Canonical Allele Identifier: CA2650532709

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441539-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441539A>G , CM000663.2:g.218441539A>G	GRCh38
NC_000001.10:g.218614881A>G , CM000663.1:g.218614881A>G	GRCh37
NC_000001.9:g.216681504A>G	NCBI36
NG_027721.1:g.101206A>G
NG_027721.2:g.101206A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*177A>G MANE Select	ENSP00000355897.4:n.*177A>G
ENST00000366929.4:c.*177A>G	ENSP00000355896.4:n.*177A>G
ENST00000366930.8:c.*177A>G	ENSP00000355897.4:n.*177A>G
ENST00000479322.1:n.906A>G
NM_001135599.2:c.*177A>G	NP_001129071.1:n.*177A>G
NM_003238.3:c.*177A>G	NP_003229.1:n.*177A>G
NM_001135599.3:c.*177A>G	NP_001129071.1:n.*177A>G
NM_003238.4:c.*177A>G	NP_003229.1:n.*177A>G
NR_138148.1:n.2725A>G
NR_138149.1:n.2809A>G
NM_003238.5:c.*177A>G	NP_003229.1:n.*177A>G
NM_003238.6:c.*177A>G MANE Select	NP_003229.1:n.*177A>G
NM_001135599.4:c.*177A>G	NP_001129071.1:n.*177A>G
NR_138148.2:n.2673A>G
NR_138149.2:n.2757A>G