Canonical Allele Identifier: CA1354873171

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672185G= , CM000665.2:g.30672185G=	GRCh38
NC_000003.11:g.30713677G= , CM000665.1:g.30713677G=	GRCh37
NC_000003.10:g.30688681G=	NCBI36
NG_007490.1:g.70684G= , LRG_779:g.70684G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1002G= MANE Select	ENSP00000295754.5:p.Gln334=
ENST00000672866.1:n.2598G=
ENST00000295754.9:c.1002G=	ENSP00000295754.5:p.Gln334=
ENST00000359013.4:c.1077G=	ENSP00000351905.4:p.Gln359=
NM_001024847.2:c.1077G= , LRG_779t1:c.1077G=	NP_001020018.1:p.Gln359=
NM_003242.5:c.1002G=	NP_003233.4:p.Gln334=
XM_011534043.1:c.1029G=	XP_011532345.1:p.Gln343=
XM_011534044.1:c.954G=	XP_011532346.1:p.Gln318=
XM_011534045.1:c.897G=	XP_011532347.1:p.Gln299=
XM_011534043.2:c.1029G=	XP_011532345.1:p.Gln343=
XM_011534045.3:c.897G=	XP_011532347.1:p.Gln299=
XM_017007106.1:c.897G=	XP_016862595.1:p.Gln299=
NM_003242.6:c.1002G= MANE Select	NP_003233.4:p.Gln334=