Canonical Allele Identifier: CA351807881

Gene: TGFBR2

Linked Data

• COSMIC: COSM3696026 ; COSM3696027
• MyVariant Identifiers: chr3:g.30713468C>T (hg19) ; chr3:g.30671976C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671976C>T , CM000665.2:g.30671976C>T	GRCh38
NC_000003.11:g.30713468C>T , CM000665.1:g.30713468C>T	GRCh37
NC_000003.10:g.30688472C>T	NCBI36
NG_007490.1:g.70475C>T , LRG_779:g.70475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.793C>T MANE Select	ENSP00000295754.5:p.Gln265Ter
ENST00000672866.1:n.2389C>T
ENST00000295754.9:c.793C>T	ENSP00000295754.5:p.Gln265Ter
ENST00000359013.4:c.868C>T	ENSP00000351905.4:p.Gln290Ter
NM_001024847.2:c.868C>T , LRG_779t1:c.868C>T	NP_001020018.1:p.Gln290Ter
NM_003242.5:c.793C>T	NP_003233.4:p.Gln265Ter
XM_011534043.1:c.820C>T	XP_011532345.1:p.Gln274Ter
XM_011534044.1:c.745C>T	XP_011532346.1:p.Gln249Ter
XM_011534045.1:c.688C>T	XP_011532347.1:p.Gln230Ter
XM_011534043.2:c.820C>T	XP_011532345.1:p.Gln274Ter
XM_011534045.3:c.688C>T	XP_011532347.1:p.Gln230Ter
XM_017007106.1:c.688C>T	XP_016862595.1:p.Gln230Ter
NM_003242.6:c.793C>T MANE Select	NP_003233.4:p.Gln265Ter