Canonical Allele Identifier: CA351807911
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1699347917

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30671990G>C , CM000665.2:g.30671990G>C GRCh38
NC_000003.11:g.30713482G>C , CM000665.1:g.30713482G>C GRCh37
NC_000003.10:g.30688486G>C NCBI36
NG_007490.1:g.70489G>C , LRG_779:g.70489G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.807G>C MANE Select ENSP00000295754.5:p.Glu269Asp
ENST00000672866.1:n.2403G>C
ENST00000295754.9:c.807G>C ENSP00000295754.5:p.Glu269Asp
ENST00000359013.4:c.882G>C ENSP00000351905.4:p.Glu294Asp
NM_001024847.2:c.882G>C , LRG_779t1:c.882G>C NP_001020018.1:p.Glu294Asp
NM_003242.5:c.807G>C NP_003233.4:p.Glu269Asp
XM_011534043.1:c.834G>C XP_011532345.1:p.Glu278Asp
XM_011534044.1:c.759G>C XP_011532346.1:p.Glu253Asp
XM_011534045.1:c.702G>C XP_011532347.1:p.Glu234Asp
XM_011534043.2:c.834G>C XP_011532345.1:p.Glu278Asp
XM_011534045.3:c.702G>C XP_011532347.1:p.Glu234Asp
XM_017007106.1:c.702G>C XP_016862595.1:p.Glu234Asp
NM_003242.6:c.807G>C MANE Select NP_003233.4:p.Glu269Asp