Canonical Allele Identifier: CA2650531271

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218346669-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346674dup , CM000663.2:g.218346674dup	GRCh38
NC_000001.10:g.218520016dup , CM000663.1:g.218520016dup	GRCh37
NC_000001.9:g.216586639dup	NCBI36
NG_027721.1:g.6341dup
NG_027721.2:g.6341dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-28dup MANE Select	ENSP00000355897.4:n.-28dup
ENST00000366929.4:c.-28dup	ENSP00000355896.4:n.-28dup
ENST00000366930.8:c.-28dup	ENSP00000355897.4:n.-28dup
NM_001135599.2:c.-28dup	NP_001129071.1:n.-28dup
NM_003238.3:c.-28dup	NP_003229.1:n.-28dup
NM_001135599.3:c.-28dup	NP_001129071.1:n.-28dup
NM_003238.4:c.-28dup	NP_003229.1:n.-28dup
NR_138148.1:n.1391dup
NR_138149.1:n.1391dup
NM_003238.5:c.-28dup	NP_003229.1:n.-28dup
NM_003238.6:c.-28dup MANE Select	NP_003229.1:n.-28dup
NM_001135599.4:c.-28dup	NP_001129071.1:n.-28dup
NR_138148.2:n.1339dup
NR_138149.2:n.1339dup