Canonical Allele Identifier: CA351807840

Gene: TGFBR2

Linked Data

• COSMIC: COSM3392331 ; COSM3392332
• MyVariant Identifiers: chr3:g.30713450T>G (hg19) ; chr3:g.30671958T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671958T>G , CM000665.2:g.30671958T>G	GRCh38
NC_000003.11:g.30713450T>G , CM000665.1:g.30713450T>G	GRCh37
NC_000003.10:g.30688454T>G	NCBI36
NG_007490.1:g.70457T>G , LRG_779:g.70457T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.775T>G MANE Select	ENSP00000295754.5:p.Tyr259Asp
ENST00000672866.1:n.2371T>G
ENST00000295754.9:c.775T>G	ENSP00000295754.5:p.Tyr259Asp
ENST00000359013.4:c.850T>G	ENSP00000351905.4:p.Tyr284Asp
NM_001024847.2:c.850T>G , LRG_779t1:c.850T>G	NP_001020018.1:p.Tyr284Asp
NM_003242.5:c.775T>G	NP_003233.4:p.Tyr259Asp
XM_011534043.1:c.802T>G	XP_011532345.1:p.Tyr268Asp
XM_011534044.1:c.727T>G	XP_011532346.1:p.Tyr243Asp
XM_011534045.1:c.670T>G	XP_011532347.1:p.Tyr224Asp
XM_011534043.2:c.802T>G	XP_011532345.1:p.Tyr268Asp
XM_011534045.3:c.670T>G	XP_011532347.1:p.Tyr224Asp
XM_017007106.1:c.670T>G	XP_016862595.1:p.Tyr224Asp
NM_003242.6:c.775T>G MANE Select	NP_003233.4:p.Tyr259Asp