Canonical Allele Identifier: CA1354873032

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671854G= , CM000665.2:g.30671854G=	GRCh38
NC_000003.11:g.30713346G= , CM000665.1:g.30713346G=	GRCh37
NC_000003.10:g.30688350G=	NCBI36
NG_007490.1:g.70353G= , LRG_779:g.70353G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.671G= MANE Select	ENSP00000295754.5:p.Arg224=
ENST00000672866.1:n.2267G=
ENST00000295754.9:c.671G=	ENSP00000295754.5:p.Arg224=
ENST00000359013.4:c.746G=	ENSP00000351905.4:p.Arg249=
NM_001024847.2:c.746G= , LRG_779t1:c.746G=	NP_001020018.1:p.Arg249=
NM_003242.5:c.671G=	NP_003233.4:p.Arg224=
XM_011534043.1:c.698G=	XP_011532345.1:p.Arg233=
XM_011534044.1:c.623G=	XP_011532346.1:p.Arg208=
XM_011534045.1:c.566G=	XP_011532347.1:p.Arg189=
XM_011534043.2:c.698G=	XP_011532345.1:p.Arg233=
XM_011534045.3:c.566G=	XP_011532347.1:p.Arg189=
XM_017007106.1:c.566G=	XP_016862595.1:p.Arg189=
NM_003242.6:c.671G= MANE Select	NP_003233.4:p.Arg224=