Canonical Allele Identifier: CA1354861067

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30645248G= , CM000665.2:g.30645248G=	GRCh38
NC_000003.11:g.30686740G= , CM000665.1:g.30686740G=	GRCh37
NC_000003.10:g.30661744G=	NCBI36
NG_007490.1:g.43747G= , LRG_779:g.43747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.263+333G= MANE Select	ENSP00000295754.5:n.263+333G=
ENST00000672866.1:n.1859+333G=
ENST00000673250.1:n.387+333G=
ENST00000295754.9:c.263+333G=	ENSP00000295754.5:n.263+333G=
ENST00000359013.4:c.338+333G=	ENSP00000351905.4:n.338+333G=
NM_001024847.2:c.338+333G= , LRG_779t1:c.338+333G=	NP_001020018.1:n.338+333G=
NM_003242.5:c.263+333G=	NP_003233.4:n.263+333G=
XM_011534043.1:c.290+333G=	XP_011532345.1:n.290+333G=
XM_011534044.1:c.215+333G=	XP_011532346.1:n.215+333G=
XM_011534045.1:c.158+333G=	XP_011532347.1:n.158+333G=
XM_011534043.2:c.290+333G=	XP_011532345.1:n.290+333G=
XM_011534045.3:c.158+333G=	XP_011532347.1:n.158+333G=
XM_017007106.1:c.158+333G=	XP_016862595.1:n.158+333G=
NM_003242.6:c.263+333G= MANE Select	NP_003233.4:n.263+333G=