Canonical Allele Identifier: CA1354873143

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672128G= , CM000665.2:g.30672128G=	GRCh38
NC_000003.11:g.30713620G= , CM000665.1:g.30713620G=	GRCh37
NC_000003.10:g.30688624G=	NCBI36
NG_007490.1:g.70627G= , LRG_779:g.70627G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.945G= MANE Select	ENSP00000295754.5:p.Thr315=
ENST00000672866.1:n.2541G=
ENST00000295754.9:c.945G=	ENSP00000295754.5:p.Thr315=
ENST00000359013.4:c.1020G=	ENSP00000351905.4:p.Thr340=
NM_001024847.2:c.1020G= , LRG_779t1:c.1020G=	NP_001020018.1:p.Thr340=
NM_003242.5:c.945G=	NP_003233.4:p.Thr315=
XM_011534043.1:c.972G=	XP_011532345.1:p.Thr324=
XM_011534044.1:c.897G=	XP_011532346.1:p.Thr299=
XM_011534045.1:c.840G=	XP_011532347.1:p.Thr280=
XM_011534043.2:c.972G=	XP_011532345.1:p.Thr324=
XM_011534045.3:c.840G=	XP_011532347.1:p.Thr280=
XM_017007106.1:c.840G=	XP_016862595.1:p.Thr280=
NM_003242.6:c.945G= MANE Select	NP_003233.4:p.Thr315=