Canonical Allele Identifier: CA2650532765

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441579-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441579_218441580insCTG , CM000663.2:g.218441579_218441580insCTG	GRCh38
NC_000001.10:g.218614921_218614922insCTG , CM000663.1:g.218614921_218614922insCTG	GRCh37
NC_000001.9:g.216681544_216681545insCTG	NCBI36
NG_027721.1:g.101246_101247insCTG
NG_027721.2:g.101246_101247insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*217_*218insCTG MANE Select	ENSP00000355897.4:n.*217_*218insCTG
ENST00000366929.4:c.*217_*218insCTG	ENSP00000355896.4:n.*217_*218insCTG
ENST00000366930.8:c.*217_*218insCTG	ENSP00000355897.4:n.*217_*218insCTG
ENST00000479322.1:n.946_947insCTG
NM_001135599.2:c.*217_*218insCTG	NP_001129071.1:n.*217_*218insCTG
NM_003238.3:c.*217_*218insCTG	NP_003229.1:n.*217_*218insCTG
NM_001135599.3:c.*217_*218insCTG	NP_001129071.1:n.*217_*218insCTG
NM_003238.4:c.*217_*218insCTG	NP_003229.1:n.*217_*218insCTG
NR_138148.1:n.2765_2766insCTG
NR_138149.1:n.2849_2850insCTG
NM_003238.5:c.*217_*218insCTG	NP_003229.1:n.*217_*218insCTG
NM_003238.6:c.*217_*218insCTG MANE Select	NP_003229.1:n.*217_*218insCTG
NM_001135599.4:c.*217_*218insCTG	NP_001129071.1:n.*217_*218insCTG
NR_138148.2:n.2713_2714insCTG
NR_138149.2:n.2797_2798insCTG