Canonical Allele Identifier: CA1354873076

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671982A= , CM000665.2:g.30671982A=	GRCh38
NC_000003.11:g.30713474A= , CM000665.1:g.30713474A=	GRCh37
NC_000003.10:g.30688478A=	NCBI36
NG_007490.1:g.70481A= , LRG_779:g.70481A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.799A= MANE Select	ENSP00000295754.5:p.Thr267=
ENST00000672866.1:n.2395A=
ENST00000295754.9:c.799A=	ENSP00000295754.5:p.Thr267=
ENST00000359013.4:c.874A=	ENSP00000351905.4:p.Thr292=
NM_001024847.2:c.874A= , LRG_779t1:c.874A=	NP_001020018.1:p.Thr292=
NM_003242.5:c.799A=	NP_003233.4:p.Thr267=
XM_011534043.1:c.826A=	XP_011532345.1:p.Thr276=
XM_011534044.1:c.751A=	XP_011532346.1:p.Thr251=
XM_011534045.1:c.694A=	XP_011532347.1:p.Thr232=
XM_011534043.2:c.826A=	XP_011532345.1:p.Thr276=
XM_011534045.3:c.694A=	XP_011532347.1:p.Thr232=
XM_017007106.1:c.694A=	XP_016862595.1:p.Thr232=
NM_003242.6:c.799A= MANE Select	NP_003233.4:p.Thr267=