Canonical Allele Identifier: CA71499877

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30644755G>A , CM000665.2:g.30644755G>A	GRCh38
NC_000003.11:g.30686247G>A , CM000665.1:g.30686247G>A	GRCh37
NC_000003.10:g.30661251G>A	NCBI36
NG_007490.1:g.43254G>A , LRG_779:g.43254G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.103G>A MANE Select	NP_003233.4:p.Asp35Asn
ENST00000295754.10:c.103G>A MANE Select	ENSP00000295754.5:p.Asp35Asn
NM_001024847.2:c.178G>A , LRG_779t1:c.178G>A	NP_001020018.1:p.Asp60Asn
NM_003242.5:c.103G>A	NP_003233.4:p.Asp35Asn
ENST00000295754.9:c.103G>A	ENSP00000295754.5:p.Asp35Asn
ENST00000359013.4:c.178G>A	ENSP00000351905.4:p.Asp60Asn
ENST00000672866.1:n.1699G>A
ENST00000673250.1:n.227G>A
XM_011534043.1:c.130G>A	XP_011532345.1:p.Asp44Asn
XM_011534043.2:c.130G>A	XP_011532345.1:p.Asp44Asn
XM_011534044.1:c.55G>A	XP_011532346.1:p.Asp19Asn
XM_011534045.1:c.-3G>A	XP_011532347.1:n.-3G>A
XM_011534045.3:c.-3G>A	XP_011532347.1:n.-3G>A
XM_017007106.1:c.-3G>A	XP_016862595.1:n.-3G>A