Canonical Allele Identifier: CA1354873963
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674066G= , CM000665.2:g.30674066G= GRCh38
NC_000003.11:g.30715558G= , CM000665.1:g.30715558G= GRCh37
NC_000003.10:g.30690562G= NCBI36
NG_007490.1:g.72565G= , LRG_779:g.72565G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1255-39G= MANE Select ENSP00000295754.5:n.1255-39G=
ENST00000672866.1:n.2851-39G=
ENST00000673203.1:n.94G=
ENST00000295754.9:c.1255-39G= ENSP00000295754.5:n.1255-39G=
ENST00000359013.4:c.1330-39G= ENSP00000351905.4:n.1330-39G=
NM_001024847.2:c.1330-39G= , LRG_779t1:c.1330-39G= NP_001020018.1:n.1330-39G=
NM_003242.5:c.1255-39G= NP_003233.4:n.1255-39G=
XM_011534043.1:c.1282-39G= XP_011532345.1:n.1282-39G=
XM_011534044.1:c.1207-39G= XP_011532346.1:n.1207-39G=
XM_011534045.1:c.1150-39G= XP_011532347.1:n.1150-39G=
XM_011534043.2:c.1282-39G= XP_011532345.1:n.1282-39G=
XM_011534045.3:c.1150-39G= XP_011532347.1:n.1150-39G=
XM_017007106.1:c.1150-39G= XP_016862595.1:n.1150-39G=
NM_003242.6:c.1255-39G= MANE Select NP_003233.4:n.1255-39G=