Canonical Allele Identifier: CA1354873256

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672353C= , CM000665.2:g.30672353C=	GRCh38
NC_000003.11:g.30713845C= , CM000665.1:g.30713845C=	GRCh37
NC_000003.10:g.30688849C=	NCBI36
NG_007490.1:g.70852C= , LRG_779:g.70852C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1170C= MANE Select	ENSP00000295754.5:p.Asp390=
ENST00000672866.1:n.2766C=
ENST00000295754.9:c.1170C=	ENSP00000295754.5:p.Asp390=
ENST00000359013.4:c.1245C=	ENSP00000351905.4:p.Asp415=
NM_001024847.2:c.1245C= , LRG_779t1:c.1245C=	NP_001020018.1:p.Asp415=
NM_003242.5:c.1170C=	NP_003233.4:p.Asp390=
XM_011534043.1:c.1197C=	XP_011532345.1:p.Asp399=
XM_011534044.1:c.1122C=	XP_011532346.1:p.Asp374=
XM_011534045.1:c.1065C=	XP_011532347.1:p.Asp355=
XM_011534043.2:c.1197C=	XP_011532345.1:p.Asp399=
XM_011534045.3:c.1065C=	XP_011532347.1:p.Asp355=
XM_017007106.1:c.1065C=	XP_016862595.1:p.Asp355=
NM_003242.6:c.1170C= MANE Select	NP_003233.4:p.Asp390=