Canonical Allele Identifier: CA2650532695

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441523-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441523_218441524insG , CM000663.2:g.218441523_218441524insG	GRCh38
NC_000001.10:g.218614865_218614866insG , CM000663.1:g.218614865_218614866insG	GRCh37
NC_000001.9:g.216681488_216681489insG	NCBI36
NG_027721.1:g.101190_101191insG
NG_027721.2:g.101190_101191insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*161_*162insG MANE Select	ENSP00000355897.4:n.*161_*162insG
ENST00000366929.4:c.*161_*162insG	ENSP00000355896.4:n.*161_*162insG
ENST00000366930.8:c.*161_*162insG	ENSP00000355897.4:n.*161_*162insG
ENST00000479322.1:n.890_891insG
NM_001135599.2:c.*161_*162insG	NP_001129071.1:n.*161_*162insG
NM_003238.3:c.*161_*162insG	NP_003229.1:n.*161_*162insG
NM_001135599.3:c.*161_*162insG	NP_001129071.1:n.*161_*162insG
NM_003238.4:c.*161_*162insG	NP_003229.1:n.*161_*162insG
NR_138148.1:n.2709_2710insG
NR_138149.1:n.2793_2794insG
NM_003238.5:c.*161_*162insG	NP_003229.1:n.*161_*162insG
NM_003238.6:c.*161_*162insG MANE Select	NP_003229.1:n.*161_*162insG
NM_001135599.4:c.*161_*162insG	NP_001129071.1:n.*161_*162insG
NR_138148.2:n.2657_2658insG
NR_138149.2:n.2741_2742insG