Canonical Allele Identifier: CA351807344

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671733A>G , CM000665.2:g.30671733A>G	GRCh38
NC_000003.11:g.30713225A>G , CM000665.1:g.30713225A>G	GRCh37
NC_000003.10:g.30688229A>G	NCBI36
NG_007490.1:g.70232A>G , LRG_779:g.70232A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.550A>G MANE Select	NP_003233.4:p.Ile184Val
ENST00000295754.10:c.550A>G MANE Select	ENSP00000295754.5:p.Ile184Val
NM_001024847.2:c.625A>G , LRG_779t1:c.625A>G	NP_001020018.1:p.Ile209Val
NM_003242.5:c.550A>G	NP_003233.4:p.Ile184Val
ENST00000295754.9:c.550A>G	ENSP00000295754.5:p.Ile184Val
ENST00000359013.4:c.625A>G	ENSP00000351905.4:p.Ile209Val
ENST00000672866.1:n.2146A>G
XM_011534043.1:c.577A>G	XP_011532345.1:p.Ile193Val
XM_011534043.2:c.577A>G	XP_011532345.1:p.Ile193Val
XM_011534044.1:c.502A>G	XP_011532346.1:p.Ile168Val
XM_011534045.1:c.445A>G	XP_011532347.1:p.Ile149Val
XM_011534045.3:c.445A>G	XP_011532347.1:p.Ile149Val
XM_017007106.1:c.445A>G	XP_016862595.1:p.Ile149Val