Canonical Allele Identifier: CA1354873209
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672255A= , CM000665.2:g.30672255A= GRCh38
NC_000003.11:g.30713747A= , CM000665.1:g.30713747A= GRCh37
NC_000003.10:g.30688751A= NCBI36
NG_007490.1:g.70754A= , LRG_779:g.70754A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1072A= MANE Select ENSP00000295754.5:p.Ile358=
ENST00000672866.1:n.2668A=
ENST00000295754.9:c.1072A= ENSP00000295754.5:p.Ile358=
ENST00000359013.4:c.1147A= ENSP00000351905.4:p.Ile383=
NM_001024847.2:c.1147A= , LRG_779t1:c.1147A= NP_001020018.1:p.Ile383=
NM_003242.5:c.1072A= NP_003233.4:p.Ile358=
XM_011534043.1:c.1099A= XP_011532345.1:p.Ile367=
XM_011534044.1:c.1024A= XP_011532346.1:p.Ile342=
XM_011534045.1:c.967A= XP_011532347.1:p.Ile323=
XM_011534043.2:c.1099A= XP_011532345.1:p.Ile367=
XM_011534045.3:c.967A= XP_011532347.1:p.Ile323=
XM_017007106.1:c.967A= XP_016862595.1:p.Ile323=
NM_003242.6:c.1072A= MANE Select NP_003233.4:p.Ile358=