Canonical Allele Identifier: CA1354881642
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30691410C= , CM000665.2:g.30691410C= GRCh38
NC_000003.11:g.30732902C= , CM000665.1:g.30732902C= GRCh37
NC_000003.10:g.30707906C= NCBI36
NG_007490.1:g.89909C= , LRG_779:g.89909C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1525-10C= MANE Select ENSP00000295754.5:n.1525-10C=
ENST00000672050.1:n.409-10C=
ENST00000672866.1:n.3121-10C=
ENST00000673203.1:n.403-10C=
ENST00000295754.9:c.1525-10C= ENSP00000295754.5:n.1525-10C=
ENST00000359013.4:c.1600-10C= ENSP00000351905.4:n.1600-10C=
NM_001024847.2:c.1600-10C= , LRG_779t1:c.1600-10C= NP_001020018.1:n.1600-10C=
NM_003242.5:c.1525-10C= NP_003233.4:n.1525-10C=
XM_011534043.1:c.1552-10C= XP_011532345.1:n.1552-10C=
XM_011534044.1:c.1477-10C= XP_011532346.1:n.1477-10C=
XM_011534045.1:c.1420-10C= XP_011532347.1:n.1420-10C=
XM_011534043.2:c.1552-10C= XP_011532345.1:n.1552-10C=
XM_011534045.3:c.1420-10C= XP_011532347.1:n.1420-10C=
XM_017007106.1:c.1420-10C= XP_016862595.1:n.1420-10C=
NM_003242.6:c.1525-10C= MANE Select NP_003233.4:n.1525-10C=