Canonical Allele Identifier: CA1354873094
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672019T= , CM000665.2:g.30672019T= GRCh38
NC_000003.11:g.30713511T= , CM000665.1:g.30713511T= GRCh37
NC_000003.10:g.30688515T= NCBI36
NG_007490.1:g.70518T= , LRG_779:g.70518T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.836T= MANE Select ENSP00000295754.5:p.Phe279=
ENST00000672866.1:n.2432T=
ENST00000295754.9:c.836T= ENSP00000295754.5:p.Phe279=
ENST00000359013.4:c.911T= ENSP00000351905.4:p.Phe304=
NM_001024847.2:c.911T= , LRG_779t1:c.911T= NP_001020018.1:p.Phe304=
NM_003242.5:c.836T= NP_003233.4:p.Phe279=
XM_011534043.1:c.863T= XP_011532345.1:p.Phe288=
XM_011534044.1:c.788T= XP_011532346.1:p.Phe263=
XM_011534045.1:c.731T= XP_011532347.1:p.Phe244=
XM_011534043.2:c.863T= XP_011532345.1:p.Phe288=
XM_011534045.3:c.731T= XP_011532347.1:p.Phe244=
XM_017007106.1:c.731T= XP_016862595.1:p.Phe244=
NM_003242.6:c.836T= MANE Select NP_003233.4:p.Phe279=