Canonical Allele Identifier: CA1354873152

Gene: TGFBR2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.964T= MANE Select	ENSP00000295754.5:p.Trp322=
ENST00000672866.1:n.2560T=
ENST00000295754.9:c.964T=	ENSP00000295754.5:p.Trp322=
ENST00000359013.4:c.1039T=	ENSP00000351905.4:p.Trp347=
NM_001024847.2:c.1039T= , LRG_779t1:c.1039T=	NP_001020018.1:p.Trp347=
NM_003242.5:c.964T=	NP_003233.4:p.Trp322=
XM_011534043.1:c.991T=	XP_011532345.1:p.Trp331=
XM_011534044.1:c.916T=	XP_011532346.1:p.Trp306=
XM_011534045.1:c.859T=	XP_011532347.1:p.Trp287=
XM_011534043.2:c.991T=	XP_011532345.1:p.Trp331=
XM_011534045.3:c.859T=	XP_011532347.1:p.Trp287=
XM_017007106.1:c.859T=	XP_016862595.1:p.Trp287=
NM_003242.6:c.964T= MANE Select	NP_003233.4:p.Trp322=