Canonical Allele Identifier: CA1354871626

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30668712C= , CM000665.2:g.30668712C=	GRCh38
NC_000003.11:g.30710204C= , CM000665.1:g.30710204C=	GRCh37
NC_000003.10:g.30685208C=	NCBI36
NG_007490.1:g.67211C= , LRG_779:g.67211C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.455-2926C= MANE Select	ENSP00000295754.5:n.455-2926C=
ENST00000672866.1:n.2051-2926C=
ENST00000295754.9:c.455-2926C=	ENSP00000295754.5:n.455-2926C=
ENST00000359013.4:c.530-2926C=	ENSP00000351905.4:n.530-2926C=
NM_001024847.2:c.530-2926C= , LRG_779t1:c.530-2926C=	NP_001020018.1:n.530-2926C=
NM_003242.5:c.455-2926C=	NP_003233.4:n.455-2926C=
XM_011534043.1:c.482-2926C=	XP_011532345.1:n.482-2926C=
XM_011534044.1:c.407-2926C=	XP_011532346.1:n.407-2926C=
XM_011534045.1:c.350-2926C=	XP_011532347.1:n.350-2926C=
XM_011534043.2:c.482-2926C=	XP_011532345.1:n.482-2926C=
XM_011534045.3:c.350-2926C=	XP_011532347.1:n.350-2926C=
XM_017007106.1:c.350-2926C=	XP_016862595.1:n.350-2926C=
NM_003242.6:c.455-2926C= MANE Select	NP_003233.4:n.455-2926C=