Canonical Allele Identifier: CA1221568470

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660149687
• gnomAD v4: 1-218441450-CATAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441452_218441456del , CM000663.2:g.218441452_218441456del	GRCh38
NC_000001.10:g.218614794_218614798del , CM000663.1:g.218614794_218614798del	GRCh37
NC_000001.9:g.216681417_216681421del	NCBI36
NG_027721.1:g.101119_101123del
NG_027721.2:g.101119_101123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*90_*94del MANE Select	ENSP00000355897.4:n.*90_*94del
ENST00000366929.4:c.*90_*94del	ENSP00000355896.4:n.*90_*94del
ENST00000366930.8:c.*90_*94del	ENSP00000355897.4:n.*90_*94del
ENST00000479322.1:n.819_823del
NM_001135599.2:c.*90_*94del	NP_001129071.1:n.*90_*94del
NM_003238.3:c.*90_*94del	NP_003229.1:n.*90_*94del
NM_001135599.3:c.*90_*94del	NP_001129071.1:n.*90_*94del
NM_003238.4:c.*90_*94del	NP_003229.1:n.*90_*94del
NR_138148.1:n.2638_2642del
NR_138149.1:n.2722_2726del
NM_003238.5:c.*90_*94del	NP_003229.1:n.*90_*94del
NM_003238.6:c.*90_*94del MANE Select	NP_003229.1:n.*90_*94del
NM_001135599.4:c.*90_*94del	NP_001129071.1:n.*90_*94del
NR_138148.2:n.2586_2590del
NR_138149.2:n.2670_2674del