Canonical Allele Identifier: CA2650531275

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218346675-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346677dup , CM000663.2:g.218346677dup	GRCh38
NC_000001.10:g.218520019dup , CM000663.1:g.218520019dup	GRCh37
NC_000001.9:g.216586642dup	NCBI36
NG_027721.1:g.6344dup
NG_027721.2:g.6344dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-25dup MANE Select	ENSP00000355897.4:n.-25dup
ENST00000366929.4:c.-25dup	ENSP00000355896.4:n.-25dup
ENST00000366930.8:c.-25dup	ENSP00000355897.4:n.-25dup
NM_001135599.2:c.-25dup	NP_001129071.1:n.-25dup
NM_003238.3:c.-25dup	NP_003229.1:n.-25dup
NM_001135599.3:c.-25dup	NP_001129071.1:n.-25dup
NM_003238.4:c.-25dup	NP_003229.1:n.-25dup
NR_138148.1:n.1394dup
NR_138149.1:n.1394dup
NM_003238.5:c.-25dup	NP_003229.1:n.-25dup
NM_003238.6:c.-25dup MANE Select	NP_003229.1:n.-25dup
NM_001135599.4:c.-25dup	NP_001129071.1:n.-25dup
NR_138148.2:n.1342dup
NR_138149.2:n.1342dup