Canonical Allele Identifier: CA1354873196

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672236C= , CM000665.2:g.30672236C=	GRCh38
NC_000003.11:g.30713728C= , CM000665.1:g.30713728C=	GRCh37
NC_000003.10:g.30688732C=	NCBI36
NG_007490.1:g.70735C= , LRG_779:g.70735C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1053C= MANE Select	ENSP00000295754.5:p.Gly351=
ENST00000672866.1:n.2649C=
ENST00000295754.9:c.1053C=	ENSP00000295754.5:p.Gly351=
ENST00000359013.4:c.1128C=	ENSP00000351905.4:p.Gly376=
NM_001024847.2:c.1128C= , LRG_779t1:c.1128C=	NP_001020018.1:p.Gly376=
NM_003242.5:c.1053C=	NP_003233.4:p.Gly351=
XM_011534043.1:c.1080C=	XP_011532345.1:p.Gly360=
XM_011534044.1:c.1005C=	XP_011532346.1:p.Gly335=
XM_011534045.1:c.948C=	XP_011532347.1:p.Gly316=
XM_011534043.2:c.1080C=	XP_011532345.1:p.Gly360=
XM_011534045.3:c.948C=	XP_011532347.1:p.Gly316=
XM_017007106.1:c.948C=	XP_016862595.1:p.Gly316=
NM_003242.6:c.1053C= MANE Select	NP_003233.4:p.Gly351=