Canonical Allele Identifier: CA1354881661

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691435T= , CM000665.2:g.30691435T=	GRCh38
NC_000003.11:g.30732927T= , CM000665.1:g.30732927T=	GRCh37
NC_000003.10:g.30707931T=	NCBI36
NG_007490.1:g.89934T= , LRG_779:g.89934T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1540T= MANE Select	NP_003233.4:p.Cys514=
ENST00000295754.10:c.1540T= MANE Select	ENSP00000295754.5:p.Cys514=
NM_001024847.2:c.1615T= , LRG_779t1:c.1615T=	NP_001020018.1:p.Cys539=
NM_003242.5:c.1540T=	NP_003233.4:p.Cys514=
ENST00000295754.9:c.1540T=	ENSP00000295754.5:p.Cys514=
ENST00000359013.4:c.1615T=	ENSP00000351905.4:p.Cys539=
ENST00000672050.1:n.424T=
ENST00000672866.1:n.3136T=
ENST00000673203.1:n.418T=
XM_011534043.1:c.1567T=	XP_011532345.1:p.Cys523=
XM_011534043.2:c.1567T=	XP_011532345.1:p.Cys523=
XM_011534044.1:c.1492T=	XP_011532346.1:p.Cys498=
XM_011534045.1:c.1435T=	XP_011532347.1:p.Cys479=
XM_011534045.3:c.1435T=	XP_011532347.1:p.Cys479=
XM_017007106.1:c.1435T=	XP_016862595.1:p.Cys479=