Canonical Allele Identifier: CA1354873264

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672373A= , CM000665.2:g.30672373A=	GRCh38
NC_000003.11:g.30713865A= , CM000665.1:g.30713865A=	GRCh37
NC_000003.10:g.30688869A=	NCBI36
NG_007490.1:g.70872A= , LRG_779:g.70872A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1190A= MANE Select	ENSP00000295754.5:p.Asp397=
ENST00000672866.1:n.2786A=
ENST00000295754.9:c.1190A=	ENSP00000295754.5:p.Asp397=
ENST00000359013.4:c.1265A=	ENSP00000351905.4:p.Asp422=
NM_001024847.2:c.1265A= , LRG_779t1:c.1265A=	NP_001020018.1:p.Asp422=
NM_003242.5:c.1190A=	NP_003233.4:p.Asp397=
XM_011534043.1:c.1217A=	XP_011532345.1:p.Asp406=
XM_011534044.1:c.1142A=	XP_011532346.1:p.Asp381=
XM_011534045.1:c.1085A=	XP_011532347.1:p.Asp362=
XM_011534043.2:c.1217A=	XP_011532345.1:p.Asp406=
XM_011534045.3:c.1085A=	XP_011532347.1:p.Asp362=
XM_017007106.1:c.1085A=	XP_016862595.1:p.Asp362=
NM_003242.6:c.1190A= MANE Select	NP_003233.4:p.Asp397=