Canonical Allele Identifier: CA1354881691

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691486G= , CM000665.2:g.30691486G=	GRCh38
NC_000003.11:g.30732978G= , CM000665.1:g.30732978G=	GRCh37
NC_000003.10:g.30707982G=	NCBI36
NG_007490.1:g.89985G= , LRG_779:g.89985G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1591G= MANE Select	NP_003233.4:p.Ala531=
ENST00000295754.10:c.1591G= MANE Select	ENSP00000295754.5:p.Ala531=
NM_001024847.2:c.1666G= , LRG_779t1:c.1666G=	NP_001020018.1:p.Ala556=
NM_003242.5:c.1591G=	NP_003233.4:p.Ala531=
ENST00000295754.9:c.1591G=	ENSP00000295754.5:p.Ala531=
ENST00000359013.4:c.1666G=	ENSP00000351905.4:p.Ala556=
ENST00000672050.1:n.475G=
ENST00000672866.1:n.3187G=
ENST00000673203.1:n.469G=
XM_011534043.1:c.1618G=	XP_011532345.1:p.Ala540=
XM_011534043.2:c.1618G=	XP_011532345.1:p.Ala540=
XM_011534044.1:c.1543G=	XP_011532346.1:p.Ala515=
XM_011534045.1:c.1486G=	XP_011532347.1:p.Ala496=
XM_011534045.3:c.1486G=	XP_011532347.1:p.Ala496=
XM_017007106.1:c.1486G=	XP_016862595.1:p.Ala496=