Canonical Allele Identifier: CA1354873075

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671980A= , CM000665.2:g.30671980A=	GRCh38
NC_000003.11:g.30713472A= , CM000665.1:g.30713472A=	GRCh37
NC_000003.10:g.30688476A=	NCBI36
NG_007490.1:g.70479A= , LRG_779:g.70479A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.797A= MANE Select	ENSP00000295754.5:p.Asn266=
ENST00000672866.1:n.2393A=
ENST00000295754.9:c.797A=	ENSP00000295754.5:p.Asn266=
ENST00000359013.4:c.872A=	ENSP00000351905.4:p.Asn291=
NM_001024847.2:c.872A= , LRG_779t1:c.872A=	NP_001020018.1:p.Asn291=
NM_003242.5:c.797A=	NP_003233.4:p.Asn266=
XM_011534043.1:c.824A=	XP_011532345.1:p.Asn275=
XM_011534044.1:c.749A=	XP_011532346.1:p.Asn250=
XM_011534045.1:c.692A=	XP_011532347.1:p.Asn231=
XM_011534043.2:c.824A=	XP_011532345.1:p.Asn275=
XM_011534045.3:c.692A=	XP_011532347.1:p.Asn231=
XM_017007106.1:c.692A=	XP_016862595.1:p.Asn231=
NM_003242.6:c.797A= MANE Select	NP_003233.4:p.Asn266=