Canonical Allele Identifier: CA1354863140

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649389G= , CM000665.2:g.30649389G=	GRCh38
NC_000003.11:g.30690881G= , CM000665.1:g.30690881G=	GRCh37
NC_000003.10:g.30665885G=	NCBI36
NG_007490.1:g.47888G= , LRG_779:g.47888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-881G= MANE Select	ENSP00000295754.5:n.264-881G=
ENST00000672866.1:n.1860-881G=
ENST00000673250.1:n.388-881G=
ENST00000295754.9:c.264-881G=	ENSP00000295754.5:n.264-881G=
ENST00000359013.4:c.339-881G=	ENSP00000351905.4:n.339-881G=
NM_001024847.2:c.339-881G= , LRG_779t1:c.339-881G=	NP_001020018.1:n.339-881G=
NM_003242.5:c.264-881G=	NP_003233.4:n.264-881G=
XM_011534043.1:c.291-881G=	XP_011532345.1:n.291-881G=
XM_011534044.1:c.216-881G=	XP_011532346.1:n.216-881G=
XM_011534045.1:c.159-881G=	XP_011532347.1:n.159-881G=
XM_011534043.2:c.291-881G=	XP_011532345.1:n.291-881G=
XM_011534045.3:c.159-881G=	XP_011532347.1:n.159-881G=
XM_017007106.1:c.159-881G=	XP_016862595.1:n.159-881G=
NM_003242.6:c.264-881G= MANE Select	NP_003233.4:n.264-881G=