Canonical Allele Identifier: CA2586965676

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674251G>T , CM000665.2:g.30674251G>T	GRCh38
NC_000003.11:g.30715743G>T , CM000665.1:g.30715743G>T	GRCh37
NC_000003.10:g.30690747G>T	NCBI36
NG_007490.1:g.72750G>T , LRG_779:g.72750G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1396+5G>T MANE Select	ENSP00000295754.5:n.1396+5G>T
ENST00000672866.1:n.2992+5G>T
ENST00000673203.1:n.274+5G>T
ENST00000295754.9:c.1396+5G>T	ENSP00000295754.5:n.1396+5G>T
ENST00000359013.4:c.1471+5G>T	ENSP00000351905.4:n.1471+5G>T
NM_001024847.2:c.1471+5G>T , LRG_779t1:c.1471+5G>T	NP_001020018.1:n.1471+5G>T
NM_003242.5:c.1396+5G>T	NP_003233.4:n.1396+5G>T
XM_011534043.1:c.1423+5G>T	XP_011532345.1:n.1423+5G>T
XM_011534044.1:c.1348+5G>T	XP_011532346.1:n.1348+5G>T
XM_011534045.1:c.1291+5G>T	XP_011532347.1:n.1291+5G>T
XM_011534043.2:c.1423+5G>T	XP_011532345.1:n.1423+5G>T
XM_011534045.3:c.1291+5G>T	XP_011532347.1:n.1291+5G>T
XM_017007106.1:c.1291+5G>T	XP_016862595.1:n.1291+5G>T
NM_003242.6:c.1396+5G>T MANE Select	NP_003233.4:n.1396+5G>T