Canonical Allele Identifier: CA1354873953
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674047G= , CM000665.2:g.30674047G= GRCh38
NC_000003.11:g.30715539G= , CM000665.1:g.30715539G= GRCh37
NC_000003.10:g.30690543G= NCBI36
NG_007490.1:g.72546G= , LRG_779:g.72546G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1255-58G= MANE Select ENSP00000295754.5:n.1255-58G=
ENST00000672866.1:n.2851-58G=
ENST00000673203.1:n.75G=
ENST00000295754.9:c.1255-58G= ENSP00000295754.5:n.1255-58G=
ENST00000359013.4:c.1330-58G= ENSP00000351905.4:n.1330-58G=
NM_001024847.2:c.1330-58G= , LRG_779t1:c.1330-58G= NP_001020018.1:n.1330-58G=
NM_003242.5:c.1255-58G= NP_003233.4:n.1255-58G=
XM_011534043.1:c.1282-58G= XP_011532345.1:n.1282-58G=
XM_011534044.1:c.1207-58G= XP_011532346.1:n.1207-58G=
XM_011534045.1:c.1150-58G= XP_011532347.1:n.1150-58G=
XM_011534043.2:c.1282-58G= XP_011532345.1:n.1282-58G=
XM_011534045.3:c.1150-58G= XP_011532347.1:n.1150-58G=
XM_017007106.1:c.1150-58G= XP_016862595.1:n.1150-58G=
NM_003242.6:c.1255-58G= MANE Select NP_003233.4:n.1255-58G=