Canonical Allele Identifier: CA432917768

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125439460
• MyVariant Identifiers: chr3:g.30715737A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674245A>G , CM000665.2:g.30674245A>G	GRCh38
NC_000003.11:g.30715737A>G , CM000665.1:g.30715737A>G	GRCh37
NC_000003.10:g.30690741A>G	NCBI36
NG_007490.1:g.72744A>G , LRG_779:g.72744A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1395A>G MANE Select	ENSP00000295754.5:p.Gly465=
ENST00000672866.1:n.2991A>G
ENST00000673203.1:n.273A>G
ENST00000295754.9:c.1395A>G	ENSP00000295754.5:p.Gly465=
ENST00000359013.4:c.1470A>G	ENSP00000351905.4:p.Gly490=
NM_001024847.2:c.1470A>G , LRG_779t1:c.1470A>G	NP_001020018.1:p.Gly490=
NM_003242.5:c.1395A>G	NP_003233.4:p.Gly465=
XM_011534043.1:c.1422A>G	XP_011532345.1:p.Gly474=
XM_011534044.1:c.1347A>G	XP_011532346.1:p.Gly449=
XM_011534045.1:c.1290A>G	XP_011532347.1:p.Gly430=
XM_011534043.2:c.1422A>G	XP_011532345.1:p.Gly474=
XM_011534045.3:c.1290A>G	XP_011532347.1:p.Gly430=
XM_017007106.1:c.1290A>G	XP_016862595.1:p.Gly430=
NM_003242.6:c.1395A>G MANE Select	NP_003233.4:p.Gly465=