Canonical Allele Identifier: CA045593

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30644758A>G , CM000665.2:g.30644758A>G	GRCh38
NC_000003.11:g.30686250A>G , CM000665.1:g.30686250A>G	GRCh37
NC_000003.10:g.30661254A>G	NCBI36
NG_007490.1:g.43257A>G , LRG_779:g.43257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.106A>G MANE Select	ENSP00000295754.5:p.Met36Val
ENST00000672866.1:n.1702A>G
ENST00000673250.1:n.230A>G
ENST00000295754.9:c.106A>G	ENSP00000295754.5:p.Met36Val
ENST00000359013.4:c.181A>G	ENSP00000351905.4:p.Met61Val
NM_001024847.2:c.181A>G , LRG_779t1:c.181A>G	NP_001020018.1:p.Met61Val
NM_003242.5:c.106A>G	NP_003233.4:p.Met36Val
XM_011534043.1:c.133A>G	XP_011532345.1:p.Met45Val
XM_011534044.1:c.58A>G	XP_011532346.1:p.Met20Val
XM_011534045.1:c.1A>G	XP_011532347.1:p.Met1Val
XM_011534043.2:c.133A>G	XP_011532345.1:p.Met45Val
XM_011534045.3:c.1A>G	XP_011532347.1:p.Met1Val
XM_017007106.1:c.1A>G	XP_016862595.1:p.Met1Val
NM_003242.6:c.106A>G MANE Select	NP_003233.4:p.Met36Val