Canonical Allele Identifier: CA1354873989

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674117A= , CM000665.2:g.30674117A=	GRCh38
NC_000003.11:g.30715609A= , CM000665.1:g.30715609A=	GRCh37
NC_000003.10:g.30690613A=	NCBI36
NG_007490.1:g.72616A= , LRG_779:g.72616A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1267A= MANE Select	ENSP00000295754.5:p.Arg423=
ENST00000672866.1:n.2863A=
ENST00000673203.1:n.145A=
ENST00000295754.9:c.1267A=	ENSP00000295754.5:p.Arg423=
ENST00000359013.4:c.1342A=	ENSP00000351905.4:p.Arg448=
NM_001024847.2:c.1342A= , LRG_779t1:c.1342A=	NP_001020018.1:p.Arg448=
NM_003242.5:c.1267A=	NP_003233.4:p.Arg423=
XM_011534043.1:c.1294A=	XP_011532345.1:p.Arg432=
XM_011534044.1:c.1219A=	XP_011532346.1:p.Arg407=
XM_011534045.1:c.1162A=	XP_011532347.1:p.Arg388=
XM_011534043.2:c.1294A=	XP_011532345.1:p.Arg432=
XM_011534045.3:c.1162A=	XP_011532347.1:p.Arg388=
XM_017007106.1:c.1162A=	XP_016862595.1:p.Arg388=
NM_003242.6:c.1267A= MANE Select	NP_003233.4:p.Arg423=