Canonical Allele Identifier: CA2664866509
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606698del , CM000665.2:g.30606698del GRCh38
NC_000003.11:g.30648190del , CM000665.1:g.30648190del GRCh37
NC_000003.10:g.30623194del NCBI36
NG_007490.1:g.5197del , LRG_779:g.5197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-186del MANE Select ENSP00000295754.5:n.-186del
ENST00000295754.9:c.-186del ENSP00000295754.5:n.-186del
ENST00000359013.4:c.-186del ENSP00000351905.4:n.-186del
NM_001024847.2:c.-186del , LRG_779t1:c.-186del NP_001020018.1:n.-186del
NM_003242.5:c.-186del NP_003233.4:n.-186del
XM_011534045.1:c.-12+105del XP_011532347.1:n.-12+105del
XM_011534045.3:c.-12+105del XP_011532347.1:n.-12+105del
NM_003242.6:c.-186del MANE Select NP_003233.4:n.-186del