Canonical Allele Identifier: CA1354873206

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672252G= , CM000665.2:g.30672252G=	GRCh38
NC_000003.11:g.30713744G= , CM000665.1:g.30713744G=	GRCh37
NC_000003.10:g.30688748G=	NCBI36
NG_007490.1:g.70751G= , LRG_779:g.70751G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1069G= MANE Select	ENSP00000295754.5:p.Gly357=
ENST00000672866.1:n.2665G=
ENST00000295754.9:c.1069G=	ENSP00000295754.5:p.Gly357=
ENST00000359013.4:c.1144G=	ENSP00000351905.4:p.Gly382=
NM_001024847.2:c.1144G= , LRG_779t1:c.1144G=	NP_001020018.1:p.Gly382=
NM_003242.5:c.1069G=	NP_003233.4:p.Gly357=
XM_011534043.1:c.1096G=	XP_011532345.1:p.Gly366=
XM_011534044.1:c.1021G=	XP_011532346.1:p.Gly341=
XM_011534045.1:c.964G=	XP_011532347.1:p.Gly322=
XM_011534043.2:c.1096G=	XP_011532345.1:p.Gly366=
XM_011534045.3:c.964G=	XP_011532347.1:p.Gly322=
XM_017007106.1:c.964G=	XP_016862595.1:p.Gly322=
NM_003242.6:c.1069G= MANE Select	NP_003233.4:p.Gly357=