Canonical Allele Identifier: CA1354873025

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671837C= , CM000665.2:g.30671837C=	GRCh38
NC_000003.11:g.30713329C= , CM000665.1:g.30713329C=	GRCh37
NC_000003.10:g.30688333C=	NCBI36
NG_007490.1:g.70336C= , LRG_779:g.70336C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.654C= MANE Select	ENSP00000295754.5:p.Ile218=
ENST00000672866.1:n.2250C=
ENST00000295754.9:c.654C=	ENSP00000295754.5:p.Ile218=
ENST00000359013.4:c.729C=	ENSP00000351905.4:p.Ile243=
NM_001024847.2:c.729C= , LRG_779t1:c.729C=	NP_001020018.1:p.Ile243=
NM_003242.5:c.654C=	NP_003233.4:p.Ile218=
XM_011534043.1:c.681C=	XP_011532345.1:p.Ile227=
XM_011534044.1:c.606C=	XP_011532346.1:p.Ile202=
XM_011534045.1:c.549C=	XP_011532347.1:p.Ile183=
XM_011534043.2:c.681C=	XP_011532345.1:p.Ile227=
XM_011534045.3:c.549C=	XP_011532347.1:p.Ile183=
XM_017007106.1:c.549C=	XP_016862595.1:p.Ile183=
NM_003242.6:c.654C= MANE Select	NP_003233.4:p.Ile218=