Canonical Allele Identifier: CA1354873029

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671850G= , CM000665.2:g.30671850G=	GRCh38
NC_000003.11:g.30713342G= , CM000665.1:g.30713342G=	GRCh37
NC_000003.10:g.30688346G=	NCBI36
NG_007490.1:g.70349G= , LRG_779:g.70349G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.667G= MANE Select	ENSP00000295754.5:p.Asp223=
ENST00000672866.1:n.2263G=
ENST00000295754.9:c.667G=	ENSP00000295754.5:p.Asp223=
ENST00000359013.4:c.742G=	ENSP00000351905.4:p.Asp248=
NM_001024847.2:c.742G= , LRG_779t1:c.742G=	NP_001020018.1:p.Asp248=
NM_003242.5:c.667G=	NP_003233.4:p.Asp223=
XM_011534043.1:c.694G=	XP_011532345.1:p.Asp232=
XM_011534044.1:c.619G=	XP_011532346.1:p.Asp207=
XM_011534045.1:c.562G=	XP_011532347.1:p.Asp188=
XM_011534043.2:c.694G=	XP_011532345.1:p.Asp232=
XM_011534045.3:c.562G=	XP_011532347.1:p.Asp188=
XM_017007106.1:c.562G=	XP_016862595.1:p.Asp188=
NM_003242.6:c.667G= MANE Select	NP_003233.4:p.Asp223=