Canonical Allele Identifier: CA71527553

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671653A>G , CM000665.2:g.30671653A>G	GRCh38
NC_000003.11:g.30713145A>G , CM000665.1:g.30713145A>G	GRCh37
NC_000003.10:g.30688149A>G	NCBI36
NG_007490.1:g.70152A>G , LRG_779:g.70152A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.470A>G MANE Select	ENSP00000295754.5:p.Asn157Ser
ENST00000672866.1:n.2066A>G
ENST00000295754.9:c.470A>G	ENSP00000295754.5:p.Asn157Ser
ENST00000359013.4:c.545A>G	ENSP00000351905.4:p.Asn182Ser
NM_001024847.2:c.545A>G , LRG_779t1:c.545A>G	NP_001020018.1:p.Asn182Ser
NM_003242.5:c.470A>G	NP_003233.4:p.Asn157Ser
XM_011534043.1:c.497A>G	XP_011532345.1:p.Asn166Ser
XM_011534044.1:c.422A>G	XP_011532346.1:p.Asn141Ser
XM_011534045.1:c.365A>G	XP_011532347.1:p.Asn122Ser
XM_011534043.2:c.497A>G	XP_011532345.1:p.Asn166Ser
XM_011534045.3:c.365A>G	XP_011532347.1:p.Asn122Ser
XM_017007106.1:c.365A>G	XP_016862595.1:p.Asn122Ser
NM_003242.6:c.470A>G MANE Select	NP_003233.4:p.Asn157Ser