Canonical Allele Identifier: CA321434

Gene: TGFBR2

Linked Data

• ClinVar Variation Id: 213944
• ClinVar RCV Id: RCV000197001
• dbSNP Id: rs863223858
• MyVariant Identifiers: chr3:g.30713639T>G (hg19) ; chr3:g.30672147T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672147T>G , CM000665.2:g.30672147T>G	GRCh38
NC_000003.11:g.30713639T>G , CM000665.1:g.30713639T>G	GRCh37
NC_000003.10:g.30688643T>G	NCBI36
NG_007490.1:g.70646T>G , LRG_779:g.70646T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.964T>G MANE Select	ENSP00000295754.5:p.Trp322Gly
ENST00000672866.1:n.2560T>G
ENST00000295754.9:c.964T>G	ENSP00000295754.5:p.Trp322Gly
ENST00000359013.4:c.1039T>G	ENSP00000351905.4:p.Trp347Gly
NM_001024847.2:c.1039T>G , LRG_779t1:c.1039T>G	NP_001020018.1:p.Trp347Gly
NM_003242.5:c.964T>G	NP_003233.4:p.Trp322Gly
XM_011534043.1:c.991T>G	XP_011532345.1:p.Trp331Gly
XM_011534044.1:c.916T>G	XP_011532346.1:p.Trp306Gly
XM_011534045.1:c.859T>G	XP_011532347.1:p.Trp287Gly
XM_011534043.2:c.991T>G	XP_011532345.1:p.Trp331Gly
XM_011534045.3:c.859T>G	XP_011532347.1:p.Trp287Gly
XM_017007106.1:c.859T>G	XP_016862595.1:p.Trp287Gly
NM_003242.6:c.964T>G MANE Select	NP_003233.4:p.Trp322Gly