Canonical Allele Identifier: CA1354873983

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674106T= , CM000665.2:g.30674106T=	GRCh38
NC_000003.11:g.30715598T= , CM000665.1:g.30715598T=	GRCh37
NC_000003.10:g.30690602T=	NCBI36
NG_007490.1:g.72605T= , LRG_779:g.72605T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1256T= MANE Select	ENSP00000295754.5:p.Val419=
ENST00000672866.1:n.2852T=
ENST00000673203.1:n.134T=
ENST00000295754.9:c.1256T=	ENSP00000295754.5:p.Val419=
ENST00000359013.4:c.1331T=	ENSP00000351905.4:p.Val444=
NM_001024847.2:c.1331T= , LRG_779t1:c.1331T=	NP_001020018.1:p.Val444=
NM_003242.5:c.1256T=	NP_003233.4:p.Val419=
XM_011534043.1:c.1283T=	XP_011532345.1:p.Val428=
XM_011534044.1:c.1208T=	XP_011532346.1:p.Val403=
XM_011534045.1:c.1151T=	XP_011532347.1:p.Val384=
XM_011534043.2:c.1283T=	XP_011532345.1:p.Val428=
XM_011534045.3:c.1151T=	XP_011532347.1:p.Val384=
XM_017007106.1:c.1151T=	XP_016862595.1:p.Val384=
NM_003242.6:c.1256T= MANE Select	NP_003233.4:p.Val419=