Canonical Allele Identifier: CA1354881700

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691505G= , CM000665.2:g.30691505G=	GRCh38
NC_000003.11:g.30732997G= , CM000665.1:g.30732997G=	GRCh37
NC_000003.10:g.30708001G=	NCBI36
NG_007490.1:g.90004G= , LRG_779:g.90004G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1610G= MANE Select	NP_003233.4:p.Arg537=
ENST00000295754.10:c.1610G= MANE Select	ENSP00000295754.5:p.Arg537=
NM_001024847.2:c.1685G= , LRG_779t1:c.1685G=	NP_001020018.1:p.Arg562=
NM_003242.5:c.1610G=	NP_003233.4:p.Arg537=
ENST00000295754.9:c.1610G=	ENSP00000295754.5:p.Arg537=
ENST00000359013.4:c.1685G=	ENSP00000351905.4:p.Arg562=
ENST00000672050.1:n.494G=
ENST00000672866.1:n.3206G=
ENST00000673203.1:n.488G=
XM_011534043.1:c.1637G=	XP_011532345.1:p.Arg546=
XM_011534043.2:c.1637G=	XP_011532345.1:p.Arg546=
XM_011534044.1:c.1562G=	XP_011532346.1:p.Arg521=
XM_011534045.1:c.1505G=	XP_011532347.1:p.Arg502=
XM_011534045.3:c.1505G=	XP_011532347.1:p.Arg502=
XM_017007106.1:c.1505G=	XP_016862595.1:p.Arg502=