Canonical Allele Identifier: CA433058790

Gene: TGFBR2

Linked Data

• dbSNP Id: rs886038794
• MyVariant Identifiers: chr3:g.30713506G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672014G>A , CM000665.2:g.30672014G>A	GRCh38
NC_000003.11:g.30713506G>A , CM000665.1:g.30713506G>A	GRCh37
NC_000003.10:g.30688510G>A	NCBI36
NG_007490.1:g.70513G>A , LRG_779:g.70513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.831G>A MANE Select	ENSP00000295754.5:p.Lys277=
ENST00000672866.1:n.2427G>A
ENST00000295754.9:c.831G>A	ENSP00000295754.5:p.Lys277=
ENST00000359013.4:c.906G>A	ENSP00000351905.4:p.Lys302=
NM_001024847.2:c.906G>A , LRG_779t1:c.906G>A	NP_001020018.1:p.Lys302=
NM_003242.5:c.831G>A	NP_003233.4:p.Lys277=
XM_011534043.1:c.858G>A	XP_011532345.1:p.Lys286=
XM_011534044.1:c.783G>A	XP_011532346.1:p.Lys261=
XM_011534045.1:c.726G>A	XP_011532347.1:p.Lys242=
XM_011534043.2:c.858G>A	XP_011532345.1:p.Lys286=
XM_011534045.3:c.726G>A	XP_011532347.1:p.Lys242=
XM_017007106.1:c.726G>A	XP_016862595.1:p.Lys242=
NM_003242.6:c.831G>A MANE Select	NP_003233.4:p.Lys277=