Canonical Allele Identifier: CA1354873098

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672026T= , CM000665.2:g.30672026T=	GRCh38
NC_000003.11:g.30713518T= , CM000665.1:g.30713518T=	GRCh37
NC_000003.10:g.30688522T=	NCBI36
NG_007490.1:g.70525T= , LRG_779:g.70525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.843T= MANE Select	ENSP00000295754.5:p.Tyr281=
ENST00000672866.1:n.2439T=
ENST00000295754.9:c.843T=	ENSP00000295754.5:p.Tyr281=
ENST00000359013.4:c.918T=	ENSP00000351905.4:p.Tyr306=
NM_001024847.2:c.918T= , LRG_779t1:c.918T=	NP_001020018.1:p.Tyr306=
NM_003242.5:c.843T=	NP_003233.4:p.Tyr281=
XM_011534043.1:c.870T=	XP_011532345.1:p.Tyr290=
XM_011534044.1:c.795T=	XP_011532346.1:p.Tyr265=
XM_011534045.1:c.738T=	XP_011532347.1:p.Tyr246=
XM_011534043.2:c.870T=	XP_011532345.1:p.Tyr290=
XM_011534045.3:c.738T=	XP_011532347.1:p.Tyr246=
XM_017007106.1:c.738T=	XP_016862595.1:p.Tyr246=
NM_003242.6:c.843T= MANE Select	NP_003233.4:p.Tyr281=