Canonical Allele Identifier: CA1354851044
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30623244G= , CM000665.2:g.30623244G= GRCh38
NC_000003.11:g.30664736G= , CM000665.1:g.30664736G= GRCh37
NC_000003.10:g.30639740G= NCBI36
NG_007490.1:g.21743G= , LRG_779:g.21743G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.94+16267G= MANE Select ENSP00000295754.5:n.94+16267G=
ENST00000673250.1:n.189G=
ENST00000295754.9:c.94+16267G= ENSP00000295754.5:n.94+16267G=
ENST00000359013.4:c.140G= ENSP00000351905.4:p.Cys47=
NM_001024847.2:c.140G= , LRG_779t1:c.140G= NP_001020018.1:p.Cys47=
NM_003242.5:c.94+16267G= NP_003233.4:n.94+16267G=
XM_011534043.1:c.92G= XP_011532345.1:p.Cys31=
XM_011534044.1:c.46+8538G= XP_011532346.1:n.46+8538G=
XM_011534045.1:c.-12+16651G= XP_011532347.1:n.-12+16651G=
XM_011534043.2:c.92G= XP_011532345.1:p.Cys31=
XM_011534045.3:c.-12+16651G= XP_011532347.1:n.-12+16651G=
NM_003242.6:c.94+16267G= MANE Select NP_003233.4:n.94+16267G=