Canonical Allele Identifier: CA1354881695

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691495G= , CM000665.2:g.30691495G=	GRCh38
NC_000003.11:g.30732987G= , CM000665.1:g.30732987G=	GRCh37
NC_000003.10:g.30707991G=	NCBI36
NG_007490.1:g.89994G= , LRG_779:g.89994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1600G= MANE Select	ENSP00000295754.5:p.Val534=
ENST00000672050.1:n.484G=
ENST00000672866.1:n.3196G=
ENST00000673203.1:n.478G=
ENST00000295754.9:c.1600G=	ENSP00000295754.5:p.Val534=
ENST00000359013.4:c.1675G=	ENSP00000351905.4:p.Val559=
NM_001024847.2:c.1675G= , LRG_779t1:c.1675G=	NP_001020018.1:p.Val559=
NM_003242.5:c.1600G=	NP_003233.4:p.Val534=
XM_011534043.1:c.1627G=	XP_011532345.1:p.Val543=
XM_011534044.1:c.1552G=	XP_011532346.1:p.Val518=
XM_011534045.1:c.1495G=	XP_011532347.1:p.Val499=
XM_011534043.2:c.1627G=	XP_011532345.1:p.Val543=
XM_011534045.3:c.1495G=	XP_011532347.1:p.Val499=
XM_017007106.1:c.1495G=	XP_016862595.1:p.Val499=
NM_003242.6:c.1600G= MANE Select	NP_003233.4:p.Val534=