Canonical Allele Identifier: CA432917986

Gene: TGFBR2

Linked Data

• dbSNP Id: rs776208827
• MyVariant Identifiers: chr3:g.30732971T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691479T>A , CM000665.2:g.30691479T>A	GRCh38
NC_000003.11:g.30732971T>A , CM000665.1:g.30732971T>A	GRCh37
NC_000003.10:g.30707975T>A	NCBI36
NG_007490.1:g.89978T>A , LRG_779:g.89978T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1584T>A MANE Select	ENSP00000295754.5:p.Arg528=
ENST00000672050.1:n.468T>A
ENST00000672866.1:n.3180T>A
ENST00000673203.1:n.462T>A
ENST00000295754.9:c.1584T>A	ENSP00000295754.5:p.Arg528=
ENST00000359013.4:c.1659T>A	ENSP00000351905.4:p.Arg553=
NM_001024847.2:c.1659T>A , LRG_779t1:c.1659T>A	NP_001020018.1:p.Arg553=
NM_003242.5:c.1584T>A	NP_003233.4:p.Arg528=
XM_011534043.1:c.1611T>A	XP_011532345.1:p.Arg537=
XM_011534044.1:c.1536T>A	XP_011532346.1:p.Arg512=
XM_011534045.1:c.1479T>A	XP_011532347.1:p.Arg493=
XM_011534043.2:c.1611T>A	XP_011532345.1:p.Arg537=
XM_011534045.3:c.1479T>A	XP_011532347.1:p.Arg493=
XM_017007106.1:c.1479T>A	XP_016862595.1:p.Arg493=
NM_003242.6:c.1584T>A MANE Select	NP_003233.4:p.Arg528=