Canonical Allele Identifier: CA351808219

Gene: TGFBR2

Linked Data

• dbSNP Id: rs34833812
• MyVariant Identifiers: chr3:g.30713619C>A (hg19) ; chr3:g.30672127C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672127C>A , CM000665.2:g.30672127C>A	GRCh38
NC_000003.11:g.30713619C>A , CM000665.1:g.30713619C>A	GRCh37
NC_000003.10:g.30688623C>A	NCBI36
NG_007490.1:g.70626C>A , LRG_779:g.70626C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.944C>A MANE Select	ENSP00000295754.5:p.Thr315Lys
ENST00000672866.1:n.2540C>A
ENST00000295754.9:c.944C>A	ENSP00000295754.5:p.Thr315Lys
ENST00000359013.4:c.1019C>A	ENSP00000351905.4:p.Thr340Lys
NM_001024847.2:c.1019C>A , LRG_779t1:c.1019C>A	NP_001020018.1:p.Thr340Lys
NM_003242.5:c.944C>A	NP_003233.4:p.Thr315Lys
XM_011534043.1:c.971C>A	XP_011532345.1:p.Thr324Lys
XM_011534044.1:c.896C>A	XP_011532346.1:p.Thr299Lys
XM_011534045.1:c.839C>A	XP_011532347.1:p.Thr280Lys
XM_011534043.2:c.971C>A	XP_011532345.1:p.Thr324Lys
XM_011534045.3:c.839C>A	XP_011532347.1:p.Thr280Lys
XM_017007106.1:c.839C>A	XP_016862595.1:p.Thr280Lys
NM_003242.6:c.944C>A MANE Select	NP_003233.4:p.Thr315Lys