Canonical Allele Identifier: CA1354866220

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30656346G= , CM000665.2:g.30656346G=	GRCh38
NC_000003.11:g.30697838G= , CM000665.1:g.30697838G=	GRCh37
NC_000003.10:g.30672842G=	NCBI36
NG_007490.1:g.54845G= , LRG_779:g.54845G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.454+5886G= MANE Select	ENSP00000295754.5:n.454+5886G=
ENST00000672866.1:n.2050+5886G=
ENST00000295754.9:c.454+5886G=	ENSP00000295754.5:n.454+5886G=
ENST00000359013.4:c.529+5886G=	ENSP00000351905.4:n.529+5886G=
NM_001024847.2:c.529+5886G= , LRG_779t1:c.529+5886G=	NP_001020018.1:n.529+5886G=
NM_003242.5:c.454+5886G=	NP_003233.4:n.454+5886G=
XM_011534043.1:c.481+5886G=	XP_011532345.1:n.481+5886G=
XM_011534044.1:c.406+5886G=	XP_011532346.1:n.406+5886G=
XM_011534045.1:c.349+5886G=	XP_011532347.1:n.349+5886G=
XR_940692.1:n.2865G=
XM_011534043.2:c.481+5886G=	XP_011532345.1:n.481+5886G=
XM_011534045.3:c.349+5886G=	XP_011532347.1:n.349+5886G=
XM_017007106.1:c.349+5886G=	XP_016862595.1:n.349+5886G=
XR_001740630.1:n.2367G=
XR_001740631.1:n.647-1361G=
NM_003242.6:c.454+5886G= MANE Select	NP_003233.4:n.454+5886G=