Canonical Allele Identifier: CA2577536088
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125438549

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606853del , CM000665.2:g.30606853del GRCh38
NC_000003.11:g.30648345del , CM000665.1:g.30648345del GRCh37
NC_000003.10:g.30623349del NCBI36
NG_007490.1:g.5352del , LRG_779:g.5352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-31del MANE Select ENSP00000295754.5:n.-31del
ENST00000295754.9:c.-31del ENSP00000295754.5:n.-31del
ENST00000359013.4:c.-31del ENSP00000351905.4:n.-31del
NM_001024847.2:c.-31del , LRG_779t1:c.-31del NP_001020018.1:n.-31del
NM_003242.5:c.-31del NP_003233.4:n.-31del
XM_011534045.1:c.-12+260del XP_011532347.1:n.-12+260del
XM_011534045.3:c.-12+260del XP_011532347.1:n.-12+260del
NM_003242.6:c.-31del MANE Select NP_003233.4:n.-31del