Canonical Allele Identifier: CA2664866569
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606753_30606765del , CM000665.2:g.30606753_30606765del GRCh38
NC_000003.11:g.30648245_30648257del , CM000665.1:g.30648245_30648257del GRCh37
NC_000003.10:g.30623249_30623261del NCBI36
NG_007490.1:g.5252_5264del , LRG_779:g.5252_5264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-131_-119del MANE Select ENSP00000295754.5:n.-131_-119del
ENST00000295754.9:c.-131_-119del ENSP00000295754.5:n.-131_-119del
ENST00000359013.4:c.-131_-119del ENSP00000351905.4:n.-131_-119del
NM_001024847.2:c.-131_-119del , LRG_779t1:c.-131_-119del NP_001020018.1:n.-131_-119del
NM_003242.5:c.-131_-119del NP_003233.4:n.-131_-119del
XM_011534045.1:c.-12+160_-12+172del XP_011532347.1:n.-12+160_-12+172del
XM_011534045.3:c.-12+160_-12+172del XP_011532347.1:n.-12+160_-12+172del
NM_003242.6:c.-131_-119del MANE Select NP_003233.4:n.-131_-119del