Canonical Allele Identifier: CA1354881686

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691478G= , CM000665.2:g.30691478G=	GRCh38
NC_000003.11:g.30732970G= , CM000665.1:g.30732970G=	GRCh37
NC_000003.10:g.30707974G=	NCBI36
NG_007490.1:g.89977G= , LRG_779:g.89977G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1583G= MANE Select	NP_003233.4:p.Arg528=
ENST00000295754.10:c.1583G= MANE Select	ENSP00000295754.5:p.Arg528=
NM_001024847.2:c.1658G= , LRG_779t1:c.1658G=	NP_001020018.1:p.Arg553=
NM_003242.5:c.1583G=	NP_003233.4:p.Arg528=
ENST00000295754.9:c.1583G=	ENSP00000295754.5:p.Arg528=
ENST00000359013.4:c.1658G=	ENSP00000351905.4:p.Arg553=
ENST00000672050.1:n.467G=
ENST00000672866.1:n.3179G=
ENST00000673203.1:n.461G=
XM_011534043.1:c.1610G=	XP_011532345.1:p.Arg537=
XM_011534043.2:c.1610G=	XP_011532345.1:p.Arg537=
XM_011534044.1:c.1535G=	XP_011532346.1:p.Arg512=
XM_011534045.1:c.1478G=	XP_011532347.1:p.Arg493=
XM_011534045.3:c.1478G=	XP_011532347.1:p.Arg493=
XM_017007106.1:c.1478G=	XP_016862595.1:p.Arg493=