Canonical Allele Identifier: CA1354873161

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672168G= , CM000665.2:g.30672168G=	GRCh38
NC_000003.11:g.30713660G= , CM000665.1:g.30713660G=	GRCh37
NC_000003.10:g.30688664G=	NCBI36
NG_007490.1:g.70667G= , LRG_779:g.70667G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.985G= MANE Select	ENSP00000295754.5:p.Ala329=
ENST00000672866.1:n.2581G=
ENST00000295754.9:c.985G=	ENSP00000295754.5:p.Ala329=
ENST00000359013.4:c.1060G=	ENSP00000351905.4:p.Ala354=
NM_001024847.2:c.1060G= , LRG_779t1:c.1060G=	NP_001020018.1:p.Ala354=
NM_003242.5:c.985G=	NP_003233.4:p.Ala329=
XM_011534043.1:c.1012G=	XP_011532345.1:p.Ala338=
XM_011534044.1:c.937G=	XP_011532346.1:p.Ala313=
XM_011534045.1:c.880G=	XP_011532347.1:p.Ala294=
XM_011534043.2:c.1012G=	XP_011532345.1:p.Ala338=
XM_011534045.3:c.880G=	XP_011532347.1:p.Ala294=
XM_017007106.1:c.880G=	XP_016862595.1:p.Ala294=
NM_003242.6:c.985G= MANE Select	NP_003233.4:p.Ala329=