Canonical Allele Identifier: CA1354880767

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30689413G= , CM000665.2:g.30689413G=	GRCh38
NC_000003.11:g.30730905G= , CM000665.1:g.30730905G=	GRCh37
NC_000003.10:g.30705909G=	NCBI36
NG_007490.1:g.87912G= , LRG_779:g.87912G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1524+902G= MANE Select	ENSP00000295754.5:n.1524+902G=
ENST00000672050.1:n.408+902G=
ENST00000672866.1:n.3120+902G=
ENST00000673203.1:n.402+902G=
ENST00000295754.9:c.1524+902G=	ENSP00000295754.5:n.1524+902G=
ENST00000359013.4:c.1599+902G=	ENSP00000351905.4:n.1599+902G=
NM_001024847.2:c.1599+902G= , LRG_779t1:c.1599+902G=	NP_001020018.1:n.1599+902G=
NM_003242.5:c.1524+902G=	NP_003233.4:n.1524+902G=
XM_011534043.1:c.1551+902G=	XP_011532345.1:n.1551+902G=
XM_011534044.1:c.1476+902G=	XP_011532346.1:n.1476+902G=
XM_011534045.1:c.1419+902G=	XP_011532347.1:n.1419+902G=
XM_011534043.2:c.1551+902G=	XP_011532345.1:n.1551+902G=
XM_011534045.3:c.1419+902G=	XP_011532347.1:n.1419+902G=
XM_017007106.1:c.1419+902G=	XP_016862595.1:n.1419+902G=
NM_003242.6:c.1524+902G= MANE Select	NP_003233.4:n.1524+902G=