Canonical Allele Identifier: CA1354873287
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672429A= , CM000665.2:g.30672429A= GRCh38
NC_000003.11:g.30713921A= , CM000665.1:g.30713921A= GRCh37
NC_000003.10:g.30688925A= NCBI36
NG_007490.1:g.70928A= , LRG_779:g.70928A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1246A= MANE Select ENSP00000295754.5:p.Ser416=
ENST00000672866.1:n.2842A=
ENST00000295754.9:c.1246A= ENSP00000295754.5:p.Ser416=
ENST00000359013.4:c.1321A= ENSP00000351905.4:p.Ser441=
NM_001024847.2:c.1321A= , LRG_779t1:c.1321A= NP_001020018.1:p.Ser441=
NM_003242.5:c.1246A= NP_003233.4:p.Ser416=
XM_011534043.1:c.1273A= XP_011532345.1:p.Ser425=
XM_011534044.1:c.1198A= XP_011532346.1:p.Ser400=
XM_011534045.1:c.1141A= XP_011532347.1:p.Ser381=
XM_011534043.2:c.1273A= XP_011532345.1:p.Ser425=
XM_011534045.3:c.1141A= XP_011532347.1:p.Ser381=
XM_017007106.1:c.1141A= XP_016862595.1:p.Ser381=
NM_003242.6:c.1246A= MANE Select NP_003233.4:p.Ser416=