Canonical Allele Identifier: CA351808022

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125434711
• MyVariant Identifiers: chr3:g.30713531T>C (hg19) ; chr3:g.30672039T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672039T>C , CM000665.2:g.30672039T>C	GRCh38
NC_000003.11:g.30713531T>C , CM000665.1:g.30713531T>C	GRCh37
NC_000003.10:g.30688535T>C	NCBI36
NG_007490.1:g.70538T>C , LRG_779:g.70538T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.856T>C MANE Select	ENSP00000295754.5:p.Ser286Pro
ENST00000672866.1:n.2452T>C
ENST00000295754.9:c.856T>C	ENSP00000295754.5:p.Ser286Pro
ENST00000359013.4:c.931T>C	ENSP00000351905.4:p.Ser311Pro
NM_001024847.2:c.931T>C , LRG_779t1:c.931T>C	NP_001020018.1:p.Ser311Pro
NM_003242.5:c.856T>C	NP_003233.4:p.Ser286Pro
XM_011534043.1:c.883T>C	XP_011532345.1:p.Ser295Pro
XM_011534044.1:c.808T>C	XP_011532346.1:p.Ser270Pro
XM_011534045.1:c.751T>C	XP_011532347.1:p.Ser251Pro
XM_011534043.2:c.883T>C	XP_011532345.1:p.Ser295Pro
XM_011534045.3:c.751T>C	XP_011532347.1:p.Ser251Pro
XM_017007106.1:c.751T>C	XP_016862595.1:p.Ser251Pro
NM_003242.6:c.856T>C MANE Select	NP_003233.4:p.Ser286Pro