Canonical Allele Identifier: CA1354863188

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649503A= , CM000665.2:g.30649503A=	GRCh38
NC_000003.11:g.30690995A= , CM000665.1:g.30690995A=	GRCh37
NC_000003.10:g.30665999A=	NCBI36
NG_007490.1:g.48002A= , LRG_779:g.48002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-767A= MANE Select	ENSP00000295754.5:n.264-767A=
ENST00000672866.1:n.1860-767A=
ENST00000673250.1:n.388-767A=
ENST00000295754.9:c.264-767A=	ENSP00000295754.5:n.264-767A=
ENST00000359013.4:c.339-767A=	ENSP00000351905.4:n.339-767A=
NM_001024847.2:c.339-767A= , LRG_779t1:c.339-767A=	NP_001020018.1:n.339-767A=
NM_003242.5:c.264-767A=	NP_003233.4:n.264-767A=
XM_011534043.1:c.291-767A=	XP_011532345.1:n.291-767A=
XM_011534044.1:c.216-767A=	XP_011532346.1:n.216-767A=
XM_011534045.1:c.159-767A=	XP_011532347.1:n.159-767A=
XM_011534043.2:c.291-767A=	XP_011532345.1:n.291-767A=
XM_011534045.3:c.159-767A=	XP_011532347.1:n.159-767A=
XM_017007106.1:c.159-767A=	XP_016862595.1:n.159-767A=
NM_003242.6:c.264-767A= MANE Select	NP_003233.4:n.264-767A=