Canonical Allele Identifier: CA1354873087

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672006G= , CM000665.2:g.30672006G=	GRCh38
NC_000003.11:g.30713498G= , CM000665.1:g.30713498G=	GRCh37
NC_000003.10:g.30688502G=	NCBI36
NG_007490.1:g.70505G= , LRG_779:g.70505G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.823G= MANE Select	ENSP00000295754.5:p.Ala275=
ENST00000672866.1:n.2419G=
ENST00000295754.9:c.823G=	ENSP00000295754.5:p.Ala275=
ENST00000359013.4:c.898G=	ENSP00000351905.4:p.Ala300=
NM_001024847.2:c.898G= , LRG_779t1:c.898G=	NP_001020018.1:p.Ala300=
NM_003242.5:c.823G=	NP_003233.4:p.Ala275=
XM_011534043.1:c.850G=	XP_011532345.1:p.Ala284=
XM_011534044.1:c.775G=	XP_011532346.1:p.Ala259=
XM_011534045.1:c.718G=	XP_011532347.1:p.Ala240=
XM_011534043.2:c.850G=	XP_011532345.1:p.Ala284=
XM_011534045.3:c.718G=	XP_011532347.1:p.Ala240=
XM_017007106.1:c.718G=	XP_016862595.1:p.Ala240=
NM_003242.6:c.823G= MANE Select	NP_003233.4:p.Ala275=