Canonical Allele Identifier: CA1354880737
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30689343A= , CM000665.2:g.30689343A= GRCh38
NC_000003.11:g.30730835A= , CM000665.1:g.30730835A= GRCh37
NC_000003.10:g.30705839A= NCBI36
NG_007490.1:g.87842A= , LRG_779:g.87842A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.1524+832A= MANE Select ENSP00000295754.5:n.1524+832A=
ENST00000672050.1:n.408+832A=
ENST00000672866.1:n.3120+832A=
ENST00000673203.1:n.402+832A=
ENST00000295754.9:c.1524+832A= ENSP00000295754.5:n.1524+832A=
ENST00000359013.4:c.1599+832A= ENSP00000351905.4:n.1599+832A=
NM_001024847.2:c.1599+832A= , LRG_779t1:c.1599+832A= NP_001020018.1:n.1599+832A=
NM_003242.5:c.1524+832A= NP_003233.4:n.1524+832A=
XM_011534043.1:c.1551+832A= XP_011532345.1:n.1551+832A=
XM_011534044.1:c.1476+832A= XP_011532346.1:n.1476+832A=
XM_011534045.1:c.1419+832A= XP_011532347.1:n.1419+832A=
XM_011534043.2:c.1551+832A= XP_011532345.1:n.1551+832A=
XM_011534045.3:c.1419+832A= XP_011532347.1:n.1419+832A=
XM_017007106.1:c.1419+832A= XP_016862595.1:n.1419+832A=
NM_003242.6:c.1524+832A= MANE Select NP_003233.4:n.1524+832A=