Canonical Allele Identifier: CA1354863165
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30649441A= , CM000665.2:g.30649441A= GRCh38
NC_000003.11:g.30690933A= , CM000665.1:g.30690933A= GRCh37
NC_000003.10:g.30665937A= NCBI36
NG_007490.1:g.47940A= , LRG_779:g.47940A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.264-829A= MANE Select ENSP00000295754.5:n.264-829A=
ENST00000672866.1:n.1860-829A=
ENST00000673250.1:n.388-829A=
ENST00000295754.9:c.264-829A= ENSP00000295754.5:n.264-829A=
ENST00000359013.4:c.339-829A= ENSP00000351905.4:n.339-829A=
NM_001024847.2:c.339-829A= , LRG_779t1:c.339-829A= NP_001020018.1:n.339-829A=
NM_003242.5:c.264-829A= NP_003233.4:n.264-829A=
XM_011534043.1:c.291-829A= XP_011532345.1:n.291-829A=
XM_011534044.1:c.216-829A= XP_011532346.1:n.216-829A=
XM_011534045.1:c.159-829A= XP_011532347.1:n.159-829A=
XM_011534043.2:c.291-829A= XP_011532345.1:n.291-829A=
XM_011534045.3:c.159-829A= XP_011532347.1:n.159-829A=
XM_017007106.1:c.159-829A= XP_016862595.1:n.159-829A=
NM_003242.6:c.264-829A= MANE Select NP_003233.4:n.264-829A=