Canonical Allele Identifier: CA1354881682

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691471G= , CM000665.2:g.30691471G=	GRCh38
NC_000003.11:g.30732963G= , CM000665.1:g.30732963G=	GRCh37
NC_000003.10:g.30707967G=	NCBI36
NG_007490.1:g.89970G= , LRG_779:g.89970G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1576G= MANE Select	ENSP00000295754.5:p.Glu526=
ENST00000672050.1:n.460G=
ENST00000672866.1:n.3172G=
ENST00000673203.1:n.454G=
ENST00000295754.9:c.1576G=	ENSP00000295754.5:p.Glu526=
ENST00000359013.4:c.1651G=	ENSP00000351905.4:p.Glu551=
NM_001024847.2:c.1651G= , LRG_779t1:c.1651G=	NP_001020018.1:p.Glu551=
NM_003242.5:c.1576G=	NP_003233.4:p.Glu526=
XM_011534043.1:c.1603G=	XP_011532345.1:p.Glu535=
XM_011534044.1:c.1528G=	XP_011532346.1:p.Glu510=
XM_011534045.1:c.1471G=	XP_011532347.1:p.Glu491=
XM_011534043.2:c.1603G=	XP_011532345.1:p.Glu535=
XM_011534045.3:c.1471G=	XP_011532347.1:p.Glu491=
XM_017007106.1:c.1471G=	XP_016862595.1:p.Glu491=
NM_003242.6:c.1576G= MANE Select	NP_003233.4:p.Glu526=