Canonical Allele Identifier: CA1354843264
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606852G= , CM000665.2:g.30606852G= GRCh38
NC_000003.11:g.30648344G= , CM000665.1:g.30648344G= GRCh37
NC_000003.10:g.30623348G= NCBI36
NG_007490.1:g.5351G= , LRG_779:g.5351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-32G= MANE Select ENSP00000295754.5:n.-32G=
ENST00000295754.9:c.-32G= ENSP00000295754.5:n.-32G=
ENST00000359013.4:c.-32G= ENSP00000351905.4:n.-32G=
NM_001024847.2:c.-32G= , LRG_779t1:c.-32G= NP_001020018.1:n.-32G=
NM_003242.5:c.-32G= NP_003233.4:n.-32G=
XM_011534045.1:c.-12+259G= XP_011532347.1:n.-12+259G=
XM_011534045.3:c.-12+259G= XP_011532347.1:n.-12+259G=
NM_003242.6:c.-32G= MANE Select NP_003233.4:n.-32G=