Canonical Allele Identifier: CA1354858545

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30639659A= , CM000665.2:g.30639659A=	GRCh38
NC_000003.11:g.30681151A= , CM000665.1:g.30681151A=	GRCh37
NC_000003.10:g.30656155A=	NCBI36
NG_007490.1:g.38158A= , LRG_779:g.38158A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.95-5088A= MANE Select	ENSP00000295754.5:n.95-5088A=
ENST00000672866.1:n.1691-5088A=
ENST00000673250.1:n.219-5088A=
ENST00000295754.9:c.95-5088A=	ENSP00000295754.5:n.95-5088A=
ENST00000359013.4:c.170-5088A=	ENSP00000351905.4:n.170-5088A=
NM_001024847.2:c.170-5088A= , LRG_779t1:c.170-5088A=	NP_001020018.1:n.170-5088A=
NM_003242.5:c.95-5088A=	NP_003233.4:n.95-5088A=
XM_011534043.1:c.122-5088A=	XP_011532345.1:n.122-5088A=
XM_011534044.1:c.47-5088A=	XP_011532346.1:n.47-5088A=
XM_011534045.1:c.-11-5088A=	XP_011532347.1:n.-11-5088A=
XM_011534043.2:c.122-5088A=	XP_011532345.1:n.122-5088A=
XM_011534045.3:c.-11-5088A=	XP_011532347.1:n.-11-5088A=
XM_017007106.1:c.-11-5088A=	XP_016862595.1:n.-11-5088A=
NM_003242.6:c.95-5088A= MANE Select	NP_003233.4:n.95-5088A=