Canonical Allele Identifier: CA433058842

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125434773
• MyVariant Identifiers: chr3:g.30713542A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672050A>G , CM000665.2:g.30672050A>G	GRCh38
NC_000003.11:g.30713542A>G , CM000665.1:g.30713542A>G	GRCh37
NC_000003.10:g.30688546A>G	NCBI36
NG_007490.1:g.70549A>G , LRG_779:g.70549A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.867A>G MANE Select	ENSP00000295754.5:p.Thr289=
ENST00000672866.1:n.2463A>G
ENST00000295754.9:c.867A>G	ENSP00000295754.5:p.Thr289=
ENST00000359013.4:c.942A>G	ENSP00000351905.4:p.Thr314=
NM_001024847.2:c.942A>G , LRG_779t1:c.942A>G	NP_001020018.1:p.Thr314=
NM_003242.5:c.867A>G	NP_003233.4:p.Thr289=
XM_011534043.1:c.894A>G	XP_011532345.1:p.Thr298=
XM_011534044.1:c.819A>G	XP_011532346.1:p.Thr273=
XM_011534045.1:c.762A>G	XP_011532347.1:p.Thr254=
XM_011534043.2:c.894A>G	XP_011532345.1:p.Thr298=
XM_011534045.3:c.762A>G	XP_011532347.1:p.Thr254=
XM_017007106.1:c.762A>G	XP_016862595.1:p.Thr254=
NM_003242.6:c.867A>G MANE Select	NP_003233.4:p.Thr289=