Canonical Allele Identifier: CA1354873180

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672200G= , CM000665.2:g.30672200G=	GRCh38
NC_000003.11:g.30713692G= , CM000665.1:g.30713692G=	GRCh37
NC_000003.10:g.30688696G=	NCBI36
NG_007490.1:g.70699G= , LRG_779:g.70699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1017G= MANE Select	ENSP00000295754.5:p.Arg339=
ENST00000672866.1:n.2613G=
ENST00000295754.9:c.1017G=	ENSP00000295754.5:p.Arg339=
ENST00000359013.4:c.1092G=	ENSP00000351905.4:p.Arg364=
NM_001024847.2:c.1092G= , LRG_779t1:c.1092G=	NP_001020018.1:p.Arg364=
NM_003242.5:c.1017G=	NP_003233.4:p.Arg339=
XM_011534043.1:c.1044G=	XP_011532345.1:p.Arg348=
XM_011534044.1:c.969G=	XP_011532346.1:p.Arg323=
XM_011534045.1:c.912G=	XP_011532347.1:p.Arg304=
XM_011534043.2:c.1044G=	XP_011532345.1:p.Arg348=
XM_011534045.3:c.912G=	XP_011532347.1:p.Arg304=
XM_017007106.1:c.912G=	XP_016862595.1:p.Arg304=
NM_003242.6:c.1017G= MANE Select	NP_003233.4:p.Arg339=