Canonical Allele Identifier: CA351808404
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125435720

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672216G>A , CM000665.2:g.30672216G>A GRCh38
NC_000003.11:g.30713708G>A , CM000665.1:g.30713708G>A GRCh37
NC_000003.10:g.30688712G>A NCBI36
NG_007490.1:g.70715G>A , LRG_779:g.70715G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1033G>A MANE Select ENSP00000295754.5:p.Glu345Lys
ENST00000672866.1:n.2629G>A
ENST00000295754.9:c.1033G>A ENSP00000295754.5:p.Glu345Lys
ENST00000359013.4:c.1108G>A ENSP00000351905.4:p.Glu370Lys
NM_001024847.2:c.1108G>A , LRG_779t1:c.1108G>A NP_001020018.1:p.Glu370Lys
NM_003242.5:c.1033G>A NP_003233.4:p.Glu345Lys
XM_011534043.1:c.1060G>A XP_011532345.1:p.Glu354Lys
XM_011534044.1:c.985G>A XP_011532346.1:p.Glu329Lys
XM_011534045.1:c.928G>A XP_011532347.1:p.Glu310Lys
XM_011534043.2:c.1060G>A XP_011532345.1:p.Glu354Lys
XM_011534045.3:c.928G>A XP_011532347.1:p.Glu310Lys
XM_017007106.1:c.928G>A XP_016862595.1:p.Glu310Lys
NM_003242.6:c.1033G>A MANE Select NP_003233.4:p.Glu345Lys