Canonical Allele Identifier: CA351807955

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1699348482
• MyVariant Identifiers: chr3:g.30713501G>A (hg19) ; chr3:g.30672009G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672009G>A , CM000665.2:g.30672009G>A	GRCh38
NC_000003.11:g.30713501G>A , CM000665.1:g.30713501G>A	GRCh37
NC_000003.10:g.30688505G>A	NCBI36
NG_007490.1:g.70508G>A , LRG_779:g.70508G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.826G>A MANE Select	ENSP00000295754.5:p.Val276Ile
ENST00000672866.1:n.2422G>A
ENST00000295754.9:c.826G>A	ENSP00000295754.5:p.Val276Ile
ENST00000359013.4:c.901G>A	ENSP00000351905.4:p.Val301Ile
NM_001024847.2:c.901G>A , LRG_779t1:c.901G>A	NP_001020018.1:p.Val301Ile
NM_003242.5:c.826G>A	NP_003233.4:p.Val276Ile
XM_011534043.1:c.853G>A	XP_011532345.1:p.Val285Ile
XM_011534044.1:c.778G>A	XP_011532346.1:p.Val260Ile
XM_011534045.1:c.721G>A	XP_011532347.1:p.Val241Ile
XM_011534043.2:c.853G>A	XP_011532345.1:p.Val285Ile
XM_011534045.3:c.721G>A	XP_011532347.1:p.Val241Ile
XM_017007106.1:c.721G>A	XP_016862595.1:p.Val241Ile
NM_003242.6:c.826G>A MANE Select	NP_003233.4:p.Val276Ile