Canonical Allele Identifier: CA351808261

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125435352
• MyVariant Identifiers: chr3:g.30713638C>A (hg19) ; chr3:g.30672146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672146C>A , CM000665.2:g.30672146C>A	GRCh38
NC_000003.11:g.30713638C>A , CM000665.1:g.30713638C>A	GRCh37
NC_000003.10:g.30688642C>A	NCBI36
NG_007490.1:g.70645C>A , LRG_779:g.70645C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.963C>A MANE Select	ENSP00000295754.5:p.Tyr321Ter
ENST00000672866.1:n.2559C>A
ENST00000295754.9:c.963C>A	ENSP00000295754.5:p.Tyr321Ter
ENST00000359013.4:c.1038C>A	ENSP00000351905.4:p.Tyr346Ter
NM_001024847.2:c.1038C>A , LRG_779t1:c.1038C>A	NP_001020018.1:p.Tyr346Ter
NM_003242.5:c.963C>A	NP_003233.4:p.Tyr321Ter
XM_011534043.1:c.990C>A	XP_011532345.1:p.Tyr330Ter
XM_011534044.1:c.915C>A	XP_011532346.1:p.Tyr305Ter
XM_011534045.1:c.858C>A	XP_011532347.1:p.Tyr286Ter
XM_011534043.2:c.990C>A	XP_011532345.1:p.Tyr330Ter
XM_011534045.3:c.858C>A	XP_011532347.1:p.Tyr286Ter
XM_017007106.1:c.858C>A	XP_016862595.1:p.Tyr286Ter
NM_003242.6:c.963C>A MANE Select	NP_003233.4:p.Tyr321Ter