Canonical Allele Identifier: CA731610174

Gene: TGFB2

Linked Data

• dbSNP Id: rs1225279594
• MyVariant Identifiers: chr1:g.218614854del (hg19) ; chr1:g.218441512del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441512del , CM000663.2:g.218441512del	GRCh38
NC_000001.10:g.218614854del , CM000663.1:g.218614854del	GRCh37
NC_000001.9:g.216681477del	NCBI36
NG_027721.1:g.101179del
NG_027721.2:g.101179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*150del MANE Select	ENSP00000355897.4:n.*150del
ENST00000366929.4:c.*150del	ENSP00000355896.4:n.*150del
ENST00000366930.8:c.*150del	ENSP00000355897.4:n.*150del
ENST00000479322.1:n.879del
NM_001135599.2:c.*150del	NP_001129071.1:n.*150del
NM_003238.3:c.*150del	NP_003229.1:n.*150del
NM_001135599.3:c.*150del	NP_001129071.1:n.*150del
NM_003238.4:c.*150del	NP_003229.1:n.*150del
NR_138148.1:n.2698del
NR_138149.1:n.2782del
NM_003238.5:c.*150del	NP_003229.1:n.*150del
NM_003238.6:c.*150del MANE Select	NP_003229.1:n.*150del
NM_001135599.4:c.*150del	NP_001129071.1:n.*150del
NR_138148.2:n.2646del
NR_138149.2:n.2730del