Canonical Allele Identifier: CA1354874040

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674243G= , CM000665.2:g.30674243G=	GRCh38
NC_000003.11:g.30715735G= , CM000665.1:g.30715735G=	GRCh37
NC_000003.10:g.30690739G=	NCBI36
NG_007490.1:g.72742G= , LRG_779:g.72742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1393G= MANE Select	ENSP00000295754.5:p.Gly465=
ENST00000672866.1:n.2989G=
ENST00000673203.1:n.271G=
ENST00000295754.9:c.1393G=	ENSP00000295754.5:p.Gly465=
ENST00000359013.4:c.1468G=	ENSP00000351905.4:p.Gly490=
NM_001024847.2:c.1468G= , LRG_779t1:c.1468G=	NP_001020018.1:p.Gly490=
NM_003242.5:c.1393G=	NP_003233.4:p.Gly465=
XM_011534043.1:c.1420G=	XP_011532345.1:p.Gly474=
XM_011534044.1:c.1345G=	XP_011532346.1:p.Gly449=
XM_011534045.1:c.1288G=	XP_011532347.1:p.Gly430=
XM_011534043.2:c.1420G=	XP_011532345.1:p.Gly474=
XM_011534045.3:c.1288G=	XP_011532347.1:p.Gly430=
XM_017007106.1:c.1288G=	XP_016862595.1:p.Gly430=
NM_003242.6:c.1393G= MANE Select	NP_003233.4:p.Gly465=