Canonical Allele Identifier: CA1354874033

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674228C= , CM000665.2:g.30674228C=	GRCh38
NC_000003.11:g.30715720C= , CM000665.1:g.30715720C=	GRCh37
NC_000003.10:g.30690724C=	NCBI36
NG_007490.1:g.72727C= , LRG_779:g.72727C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1378C= MANE Select	NP_003233.4:p.Arg460=
ENST00000295754.10:c.1378C= MANE Select	ENSP00000295754.5:p.Arg460=
NM_001024847.2:c.1453C= , LRG_779t1:c.1453C=	NP_001020018.1:p.Arg485=
NM_003242.5:c.1378C=	NP_003233.4:p.Arg460=
ENST00000295754.9:c.1378C=	ENSP00000295754.5:p.Arg460=
ENST00000359013.4:c.1453C=	ENSP00000351905.4:p.Arg485=
ENST00000672866.1:n.2974C=
ENST00000673203.1:n.256C=
XM_011534043.1:c.1405C=	XP_011532345.1:p.Arg469=
XM_011534043.2:c.1405C=	XP_011532345.1:p.Arg469=
XM_011534044.1:c.1330C=	XP_011532346.1:p.Arg444=
XM_011534045.1:c.1273C=	XP_011532347.1:p.Arg425=
XM_011534045.3:c.1273C=	XP_011532347.1:p.Arg425=
XM_017007106.1:c.1273C=	XP_016862595.1:p.Arg425=