Canonical Allele Identifier: CA351808022
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125434711

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672039T>C , CM000665.2:g.30672039T>C GRCh38
NC_000003.11:g.30713531T>C , CM000665.1:g.30713531T>C GRCh37
NC_000003.10:g.30688535T>C NCBI36
NG_007490.1:g.70538T>C , LRG_779:g.70538T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.856T>C MANE Select ENSP00000295754.5:p.Ser286Pro
ENST00000672866.1:n.2452T>C
ENST00000295754.9:c.856T>C ENSP00000295754.5:p.Ser286Pro
ENST00000359013.4:c.931T>C ENSP00000351905.4:p.Ser311Pro
NM_001024847.2:c.931T>C , LRG_779t1:c.931T>C NP_001020018.1:p.Ser311Pro
NM_003242.5:c.856T>C NP_003233.4:p.Ser286Pro
XM_011534043.1:c.883T>C XP_011532345.1:p.Ser295Pro
XM_011534044.1:c.808T>C XP_011532346.1:p.Ser270Pro
XM_011534045.1:c.751T>C XP_011532347.1:p.Ser251Pro
XM_011534043.2:c.883T>C XP_011532345.1:p.Ser295Pro
XM_011534045.3:c.751T>C XP_011532347.1:p.Ser251Pro
XM_017007106.1:c.751T>C XP_016862595.1:p.Ser251Pro
NM_003242.6:c.856T>C MANE Select NP_003233.4:p.Ser286Pro