Canonical Allele Identifier: CA1354843167
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606711C= , CM000665.2:g.30606711C= GRCh38
NC_000003.11:g.30648203C= , CM000665.1:g.30648203C= GRCh37
NC_000003.10:g.30623207C= NCBI36
NG_007490.1:g.5210C= , LRG_779:g.5210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-173C= MANE Select ENSP00000295754.5:n.-173C=
ENST00000295754.9:c.-173C= ENSP00000295754.5:n.-173C=
ENST00000359013.4:c.-173C= ENSP00000351905.4:n.-173C=
NM_001024847.2:c.-173C= , LRG_779t1:c.-173C= NP_001020018.1:n.-173C=
NM_003242.5:c.-173C= NP_003233.4:n.-173C=
XM_011534045.1:c.-12+118C= XP_011532347.1:n.-12+118C=
XM_011534045.3:c.-12+118C= XP_011532347.1:n.-12+118C=
NM_003242.6:c.-173C= MANE Select NP_003233.4:n.-173C=