Canonical Allele Identifier: CA731610213

Gene: TGFB2

Linked Data

• dbSNP Id: rs1226428581
• MyVariant Identifiers: chr1:g.218614939_218614942del (hg19) ; chr1:g.218441597_218441600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441599_218441602del , CM000663.2:g.218441599_218441602del	GRCh38
NC_000001.10:g.218614941_218614944del , CM000663.1:g.218614941_218614944del	GRCh37
NC_000001.9:g.216681564_216681567del	NCBI36
NG_027721.1:g.101266_101269del
NG_027721.2:g.101266_101269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*237_*240del MANE Select	ENSP00000355897.4:n.*237_*240del
ENST00000366929.4:c.*237_*240del	ENSP00000355896.4:n.*237_*240del
ENST00000366930.8:c.*237_*240del	ENSP00000355897.4:n.*237_*240del
ENST00000479322.1:n.966_969del
NM_001135599.2:c.*237_*240del	NP_001129071.1:n.*237_*240del
NM_003238.3:c.*237_*240del	NP_003229.1:n.*237_*240del
NM_001135599.3:c.*237_*240del	NP_001129071.1:n.*237_*240del
NM_003238.4:c.*237_*240del	NP_003229.1:n.*237_*240del
NR_138148.1:n.2785_2788del
NR_138149.1:n.2869_2872del
NM_003238.5:c.*237_*240del	NP_003229.1:n.*237_*240del
NM_003238.6:c.*237_*240del MANE Select	NP_003229.1:n.*237_*240del
NM_001135599.4:c.*237_*240del	NP_001129071.1:n.*237_*240del
NR_138148.2:n.2733_2736del
NR_138149.2:n.2817_2820del