Canonical Allele Identifier: CA433059005

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125435684
• MyVariant Identifiers: chr3:g.30713698C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672206C>A , CM000665.2:g.30672206C>A	GRCh38
NC_000003.11:g.30713698C>A , CM000665.1:g.30713698C>A	GRCh37
NC_000003.10:g.30688702C>A	NCBI36
NG_007490.1:g.70705C>A , LRG_779:g.70705C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1023C>A MANE Select	ENSP00000295754.5:p.Val341=
ENST00000672866.1:n.2619C>A
ENST00000295754.9:c.1023C>A	ENSP00000295754.5:p.Val341=
ENST00000359013.4:c.1098C>A	ENSP00000351905.4:p.Val366=
NM_001024847.2:c.1098C>A , LRG_779t1:c.1098C>A	NP_001020018.1:p.Val366=
NM_003242.5:c.1023C>A	NP_003233.4:p.Val341=
XM_011534043.1:c.1050C>A	XP_011532345.1:p.Val350=
XM_011534044.1:c.975C>A	XP_011532346.1:p.Val325=
XM_011534045.1:c.918C>A	XP_011532347.1:p.Val306=
XM_011534043.2:c.1050C>A	XP_011532345.1:p.Val350=
XM_011534045.3:c.918C>A	XP_011532347.1:p.Val306=
XM_017007106.1:c.918C>A	XP_016862595.1:p.Val306=
NM_003242.6:c.1023C>A MANE Select	NP_003233.4:p.Val341=