Canonical Allele Identifier: CA1354873085

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672004T= , CM000665.2:g.30672004T=	GRCh38
NC_000003.11:g.30713496T= , CM000665.1:g.30713496T=	GRCh37
NC_000003.10:g.30688500T=	NCBI36
NG_007490.1:g.70503T= , LRG_779:g.70503T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.821T= MANE Select	ENSP00000295754.5:p.Val274=
ENST00000672866.1:n.2417T=
ENST00000295754.9:c.821T=	ENSP00000295754.5:p.Val274=
ENST00000359013.4:c.896T=	ENSP00000351905.4:p.Val299=
NM_001024847.2:c.896T= , LRG_779t1:c.896T=	NP_001020018.1:p.Val299=
NM_003242.5:c.821T=	NP_003233.4:p.Val274=
XM_011534043.1:c.848T=	XP_011532345.1:p.Val283=
XM_011534044.1:c.773T=	XP_011532346.1:p.Val258=
XM_011534045.1:c.716T=	XP_011532347.1:p.Val239=
XM_011534043.2:c.848T=	XP_011532345.1:p.Val283=
XM_011534045.3:c.716T=	XP_011532347.1:p.Val239=
XM_017007106.1:c.716T=	XP_016862595.1:p.Val239=
NM_003242.6:c.821T= MANE Select	NP_003233.4:p.Val274=