Canonical Allele Identifier: CA351808350
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672188G>T , CM000665.2:g.30672188G>T GRCh38
NC_000003.11:g.30713680G>T , CM000665.1:g.30713680G>T GRCh37
NC_000003.10:g.30688684G>T NCBI36
NG_007490.1:g.70687G>T , LRG_779:g.70687G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1005G>T MANE Select ENSP00000295754.5:p.Glu335Asp
ENST00000672866.1:n.2601G>T
ENST00000295754.9:c.1005G>T ENSP00000295754.5:p.Glu335Asp
ENST00000359013.4:c.1080G>T ENSP00000351905.4:p.Glu360Asp
NM_001024847.2:c.1080G>T , LRG_779t1:c.1080G>T NP_001020018.1:p.Glu360Asp
NM_003242.5:c.1005G>T NP_003233.4:p.Glu335Asp
XM_011534043.1:c.1032G>T XP_011532345.1:p.Glu344Asp
XM_011534044.1:c.957G>T XP_011532346.1:p.Glu319Asp
XM_011534045.1:c.900G>T XP_011532347.1:p.Glu300Asp
XM_011534043.2:c.1032G>T XP_011532345.1:p.Glu344Asp
XM_011534045.3:c.900G>T XP_011532347.1:p.Glu300Asp
XM_017007106.1:c.900G>T XP_016862595.1:p.Glu300Asp
NM_003242.6:c.1005G>T MANE Select NP_003233.4:p.Glu335Asp