Canonical Allele Identifier: CA1354873130
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672106T= , CM000665.2:g.30672106T= GRCh38
NC_000003.11:g.30713598T= , CM000665.1:g.30713598T= GRCh37
NC_000003.10:g.30688602T= NCBI36
NG_007490.1:g.70605T= , LRG_779:g.70605T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.923T= MANE Select ENSP00000295754.5:p.Leu308=
ENST00000672866.1:n.2519T=
ENST00000295754.9:c.923T= ENSP00000295754.5:p.Leu308=
ENST00000359013.4:c.998T= ENSP00000351905.4:p.Leu333=
NM_001024847.2:c.998T= , LRG_779t1:c.998T= NP_001020018.1:p.Leu333=
NM_003242.5:c.923T= NP_003233.4:p.Leu308=
XM_011534043.1:c.950T= XP_011532345.1:p.Leu317=
XM_011534044.1:c.875T= XP_011532346.1:p.Leu292=
XM_011534045.1:c.818T= XP_011532347.1:p.Leu273=
XM_011534043.2:c.950T= XP_011532345.1:p.Leu317=
XM_011534045.3:c.818T= XP_011532347.1:p.Leu273=
XM_017007106.1:c.818T= XP_016862595.1:p.Leu273=
NM_003242.6:c.923T= MANE Select NP_003233.4:p.Leu308=