Canonical Allele Identifier: CA1354871576

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1699284261

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30668585_30668586insC , CM000665.2:g.30668585_30668586insC	GRCh38
NC_000003.11:g.30710077_30710078insC , CM000665.1:g.30710077_30710078insC	GRCh37
NC_000003.10:g.30685081_30685082insC	NCBI36
NG_007490.1:g.67084_67085insC , LRG_779:g.67084_67085insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.455-3053_455-3052insC MANE Select	ENSP00000295754.5:n.455-3053_455-3052insC
ENST00000672866.1:n.2051-3053_2051-3052insC
ENST00000295754.9:c.455-3053_455-3052insC	ENSP00000295754.5:n.455-3053_455-3052insC
ENST00000359013.4:c.530-3053_530-3052insC	ENSP00000351905.4:n.530-3053_530-3052insC
NM_001024847.2:c.530-3053_530-3052insC , LRG_779t1:c.530-3053_530-3052insC	NP_001020018.1:n.530-3053_530-3052insC
NM_003242.5:c.455-3053_455-3052insC	NP_003233.4:n.455-3053_455-3052insC
XM_011534043.1:c.482-3053_482-3052insC	XP_011532345.1:n.482-3053_482-3052insC
XM_011534044.1:c.407-3053_407-3052insC	XP_011532346.1:n.407-3053_407-3052insC
XM_011534045.1:c.350-3053_350-3052insC	XP_011532347.1:n.350-3053_350-3052insC
XM_011534043.2:c.482-3053_482-3052insC	XP_011532345.1:n.482-3053_482-3052insC
XM_011534045.3:c.350-3053_350-3052insC	XP_011532347.1:n.350-3053_350-3052insC
XM_017007106.1:c.350-3053_350-3052insC	XP_016862595.1:n.350-3053_350-3052insC
NM_003242.6:c.455-3053_455-3052insC MANE Select	NP_003233.4:n.455-3053_455-3052insC