Canonical Allele Identifier: CA1354873263

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672372G= , CM000665.2:g.30672372G=	GRCh38
NC_000003.11:g.30713864G= , CM000665.1:g.30713864G=	GRCh37
NC_000003.10:g.30688868G=	NCBI36
NG_007490.1:g.70871G= , LRG_779:g.70871G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1189G= MANE Select	ENSP00000295754.5:p.Asp397=
ENST00000672866.1:n.2785G=
ENST00000295754.9:c.1189G=	ENSP00000295754.5:p.Asp397=
ENST00000359013.4:c.1264G=	ENSP00000351905.4:p.Asp422=
NM_001024847.2:c.1264G= , LRG_779t1:c.1264G=	NP_001020018.1:p.Asp422=
NM_003242.5:c.1189G=	NP_003233.4:p.Asp397=
XM_011534043.1:c.1216G=	XP_011532345.1:p.Asp406=
XM_011534044.1:c.1141G=	XP_011532346.1:p.Asp381=
XM_011534045.1:c.1084G=	XP_011532347.1:p.Asp362=
XM_011534043.2:c.1216G=	XP_011532345.1:p.Asp406=
XM_011534045.3:c.1084G=	XP_011532347.1:p.Asp362=
XM_017007106.1:c.1084G=	XP_016862595.1:p.Asp362=
NM_003242.6:c.1189G= MANE Select	NP_003233.4:p.Asp397=