Canonical Allele Identifier: CA433058357

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30713362C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671870C>A , CM000665.2:g.30671870C>A	GRCh38
NC_000003.11:g.30713362C>A , CM000665.1:g.30713362C>A	GRCh37
NC_000003.10:g.30688366C>A	NCBI36
NG_007490.1:g.70369C>A , LRG_779:g.70369C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.687C>A MANE Select	ENSP00000295754.5:p.Ser229=
ENST00000672866.1:n.2283C>A
ENST00000295754.9:c.687C>A	ENSP00000295754.5:p.Ser229=
ENST00000359013.4:c.762C>A	ENSP00000351905.4:p.Ser254=
NM_001024847.2:c.762C>A , LRG_779t1:c.762C>A	NP_001020018.1:p.Ser254=
NM_003242.5:c.687C>A	NP_003233.4:p.Ser229=
XM_011534043.1:c.714C>A	XP_011532345.1:p.Ser238=
XM_011534044.1:c.639C>A	XP_011532346.1:p.Ser213=
XM_011534045.1:c.582C>A	XP_011532347.1:p.Ser194=
XM_011534043.2:c.714C>A	XP_011532345.1:p.Ser238=
XM_011534045.3:c.582C>A	XP_011532347.1:p.Ser194=
XM_017007106.1:c.582C>A	XP_016862595.1:p.Ser194=
NM_003242.6:c.687C>A MANE Select	NP_003233.4:p.Ser229=