Canonical Allele Identifier: CA432917618

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1699359661
• MyVariant Identifiers: chr3:g.30713851C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672359C>A , CM000665.2:g.30672359C>A	GRCh38
NC_000003.11:g.30713851C>A , CM000665.1:g.30713851C>A	GRCh37
NC_000003.10:g.30688855C>A	NCBI36
NG_007490.1:g.70858C>A , LRG_779:g.70858C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1176C>A MANE Select	ENSP00000295754.5:p.Thr392=
ENST00000672866.1:n.2772C>A
ENST00000295754.9:c.1176C>A	ENSP00000295754.5:p.Thr392=
ENST00000359013.4:c.1251C>A	ENSP00000351905.4:p.Thr417=
NM_001024847.2:c.1251C>A , LRG_779t1:c.1251C>A	NP_001020018.1:p.Thr417=
NM_003242.5:c.1176C>A	NP_003233.4:p.Thr392=
XM_011534043.1:c.1203C>A	XP_011532345.1:p.Thr401=
XM_011534044.1:c.1128C>A	XP_011532346.1:p.Thr376=
XM_011534045.1:c.1071C>A	XP_011532347.1:p.Thr357=
XM_011534043.2:c.1203C>A	XP_011532345.1:p.Thr401=
XM_011534045.3:c.1071C>A	XP_011532347.1:p.Thr357=
XM_017007106.1:c.1071C>A	XP_016862595.1:p.Thr357=
NM_003242.6:c.1176C>A MANE Select	NP_003233.4:p.Thr392=