Canonical Allele Identifier: CA1354873067

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671951T= , CM000665.2:g.30671951T=	GRCh38
NC_000003.11:g.30713443T= , CM000665.1:g.30713443T=	GRCh37
NC_000003.10:g.30688447T=	NCBI36
NG_007490.1:g.70450T= , LRG_779:g.70450T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.768T= MANE Select	ENSP00000295754.5:p.Ala256=
ENST00000672866.1:n.2364T=
ENST00000295754.9:c.768T=	ENSP00000295754.5:p.Ala256=
ENST00000359013.4:c.843T=	ENSP00000351905.4:p.Ala281=
NM_001024847.2:c.843T= , LRG_779t1:c.843T=	NP_001020018.1:p.Ala281=
NM_003242.5:c.768T=	NP_003233.4:p.Ala256=
XM_011534043.1:c.795T=	XP_011532345.1:p.Ala265=
XM_011534044.1:c.720T=	XP_011532346.1:p.Ala240=
XM_011534045.1:c.663T=	XP_011532347.1:p.Ala221=
XM_011534043.2:c.795T=	XP_011532345.1:p.Ala265=
XM_011534045.3:c.663T=	XP_011532347.1:p.Ala221=
XM_017007106.1:c.663T=	XP_016862595.1:p.Ala221=
NM_003242.6:c.768T= MANE Select	NP_003233.4:p.Ala256=