Canonical Allele Identifier: CA321058

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30650443A>G , CM000665.2:g.30650443A>G	GRCh38
NC_000003.11:g.30691935A>G , CM000665.1:g.30691935A>G	GRCh37
NC_000003.10:g.30666939A>G	NCBI36
NG_007490.1:g.48942A>G , LRG_779:g.48942A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.437A>G MANE Select	ENSP00000295754.5:p.Asn146Ser
ENST00000672866.1:n.2033A>G
ENST00000673250.1:n.561A>G
ENST00000295754.9:c.437A>G	ENSP00000295754.5:p.Asn146Ser
ENST00000359013.4:c.512A>G	ENSP00000351905.4:p.Asn171Ser
NM_001024847.2:c.512A>G , LRG_779t1:c.512A>G	NP_001020018.1:p.Asn171Ser
NM_003242.5:c.437A>G	NP_003233.4:p.Asn146Ser
XM_011534043.1:c.464A>G	XP_011532345.1:p.Asn155Ser
XM_011534044.1:c.389A>G	XP_011532346.1:p.Asn130Ser
XM_011534045.1:c.332A>G	XP_011532347.1:p.Asn111Ser
XM_011534043.2:c.464A>G	XP_011532345.1:p.Asn155Ser
XM_011534045.3:c.332A>G	XP_011532347.1:p.Asn111Ser
XM_017007106.1:c.332A>G	XP_016862595.1:p.Asn111Ser
NM_003242.6:c.437A>G MANE Select	NP_003233.4:p.Asn146Ser