Canonical Allele Identifier: CA1354873205
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672251G= , CM000665.2:g.30672251G= GRCh38
NC_000003.11:g.30713743G= , CM000665.1:g.30713743G= GRCh37
NC_000003.10:g.30688747G= NCBI36
NG_007490.1:g.70750G= , LRG_779:g.70750G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1068G= MANE Select ENSP00000295754.5:p.Arg356=
ENST00000672866.1:n.2664G=
ENST00000295754.9:c.1068G= ENSP00000295754.5:p.Arg356=
ENST00000359013.4:c.1143G= ENSP00000351905.4:p.Arg381=
NM_001024847.2:c.1143G= , LRG_779t1:c.1143G= NP_001020018.1:p.Arg381=
NM_003242.5:c.1068G= NP_003233.4:p.Arg356=
XM_011534043.1:c.1095G= XP_011532345.1:p.Arg365=
XM_011534044.1:c.1020G= XP_011532346.1:p.Arg340=
XM_011534045.1:c.963G= XP_011532347.1:p.Arg321=
XM_011534043.2:c.1095G= XP_011532345.1:p.Arg365=
XM_011534045.3:c.963G= XP_011532347.1:p.Arg321=
XM_017007106.1:c.963G= XP_016862595.1:p.Arg321=
NM_003242.6:c.1068G= MANE Select NP_003233.4:p.Arg356=