Canonical Allele Identifier: CA1354873047

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671907C= , CM000665.2:g.30671907C=	GRCh38
NC_000003.11:g.30713399C= , CM000665.1:g.30713399C=	GRCh37
NC_000003.10:g.30688403C=	NCBI36
NG_007490.1:g.70406C= , LRG_779:g.70406C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.724C= MANE Select	ENSP00000295754.5:p.Leu242=
ENST00000672866.1:n.2320C=
ENST00000295754.9:c.724C=	ENSP00000295754.5:p.Leu242=
ENST00000359013.4:c.799C=	ENSP00000351905.4:p.Leu267=
NM_001024847.2:c.799C= , LRG_779t1:c.799C=	NP_001020018.1:p.Leu267=
NM_003242.5:c.724C=	NP_003233.4:p.Leu242=
XM_011534043.1:c.751C=	XP_011532345.1:p.Leu251=
XM_011534044.1:c.676C=	XP_011532346.1:p.Leu226=
XM_011534045.1:c.619C=	XP_011532347.1:p.Leu207=
XM_011534043.2:c.751C=	XP_011532345.1:p.Leu251=
XM_011534045.3:c.619C=	XP_011532347.1:p.Leu207=
XM_017007106.1:c.619C=	XP_016862595.1:p.Leu207=
NM_003242.6:c.724C= MANE Select	NP_003233.4:p.Leu242=