Canonical Allele Identifier: CA433059019

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125435728
• MyVariant Identifiers: chr3:g.30713710G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672218G>A , CM000665.2:g.30672218G>A	GRCh38
NC_000003.11:g.30713710G>A , CM000665.1:g.30713710G>A	GRCh37
NC_000003.10:g.30688714G>A	NCBI36
NG_007490.1:g.70717G>A , LRG_779:g.70717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1035G>A MANE Select	ENSP00000295754.5:p.Glu345=
ENST00000672866.1:n.2631G>A
ENST00000295754.9:c.1035G>A	ENSP00000295754.5:p.Glu345=
ENST00000359013.4:c.1110G>A	ENSP00000351905.4:p.Glu370=
NM_001024847.2:c.1110G>A , LRG_779t1:c.1110G>A	NP_001020018.1:p.Glu370=
NM_003242.5:c.1035G>A	NP_003233.4:p.Glu345=
XM_011534043.1:c.1062G>A	XP_011532345.1:p.Glu354=
XM_011534044.1:c.987G>A	XP_011532346.1:p.Glu329=
XM_011534045.1:c.930G>A	XP_011532347.1:p.Glu310=
XM_011534043.2:c.1062G>A	XP_011532345.1:p.Glu354=
XM_011534045.3:c.930G>A	XP_011532347.1:p.Glu310=
XM_017007106.1:c.930G>A	XP_016862595.1:p.Glu310=
NM_003242.6:c.1035G>A MANE Select	NP_003233.4:p.Glu345=