Canonical Allele Identifier: CA2702374021

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125438674

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674093T>G , CM000665.2:g.30674093T>G	GRCh38
NC_000003.11:g.30715585T>G , CM000665.1:g.30715585T>G	GRCh37
NC_000003.10:g.30690589T>G	NCBI36
NG_007490.1:g.72592T>G , LRG_779:g.72592T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1255-12T>G MANE Select	ENSP00000295754.5:n.1255-12T>G
ENST00000672866.1:n.2851-12T>G
ENST00000673203.1:n.121T>G
ENST00000295754.9:c.1255-12T>G	ENSP00000295754.5:n.1255-12T>G
ENST00000359013.4:c.1330-12T>G	ENSP00000351905.4:n.1330-12T>G
NM_001024847.2:c.1330-12T>G , LRG_779t1:c.1330-12T>G	NP_001020018.1:n.1330-12T>G
NM_003242.5:c.1255-12T>G	NP_003233.4:n.1255-12T>G
XM_011534043.1:c.1282-12T>G	XP_011532345.1:n.1282-12T>G
XM_011534044.1:c.1207-12T>G	XP_011532346.1:n.1207-12T>G
XM_011534045.1:c.1150-12T>G	XP_011532347.1:n.1150-12T>G
XM_011534043.2:c.1282-12T>G	XP_011532345.1:n.1282-12T>G
XM_011534045.3:c.1150-12T>G	XP_011532347.1:n.1150-12T>G
XM_017007106.1:c.1150-12T>G	XP_016862595.1:n.1150-12T>G
NM_003242.6:c.1255-12T>G MANE Select	NP_003233.4:n.1255-12T>G