Canonical Allele Identifier: CA1354873160

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672167C= , CM000665.2:g.30672167C=	GRCh38
NC_000003.11:g.30713659C= , CM000665.1:g.30713659C=	GRCh37
NC_000003.10:g.30688663C=	NCBI36
NG_007490.1:g.70666C= , LRG_779:g.70666C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.984C= MANE Select	ENSP00000295754.5:p.His328=
ENST00000672866.1:n.2580C=
ENST00000295754.9:c.984C=	ENSP00000295754.5:p.His328=
ENST00000359013.4:c.1059C=	ENSP00000351905.4:p.His353=
NM_001024847.2:c.1059C= , LRG_779t1:c.1059C=	NP_001020018.1:p.His353=
NM_003242.5:c.984C=	NP_003233.4:p.His328=
XM_011534043.1:c.1011C=	XP_011532345.1:p.His337=
XM_011534044.1:c.936C=	XP_011532346.1:p.His312=
XM_011534045.1:c.879C=	XP_011532347.1:p.His293=
XM_011534043.2:c.1011C=	XP_011532345.1:p.His337=
XM_011534045.3:c.879C=	XP_011532347.1:p.His293=
XM_017007106.1:c.879C=	XP_016862595.1:p.His293=
NM_003242.6:c.984C= MANE Select	NP_003233.4:p.His328=