Canonical Allele Identifier: CA351808002

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125434662
• MyVariant Identifiers: chr3:g.30713522G>C (hg19) ; chr3:g.30672030G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672030G>C , CM000665.2:g.30672030G>C	GRCh38
NC_000003.11:g.30713522G>C , CM000665.1:g.30713522G>C	GRCh37
NC_000003.10:g.30688526G>C	NCBI36
NG_007490.1:g.70529G>C , LRG_779:g.70529G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.847G>C MANE Select	ENSP00000295754.5:p.Glu283Gln
ENST00000672866.1:n.2443G>C
ENST00000295754.9:c.847G>C	ENSP00000295754.5:p.Glu283Gln
ENST00000359013.4:c.922G>C	ENSP00000351905.4:p.Glu308Gln
NM_001024847.2:c.922G>C , LRG_779t1:c.922G>C	NP_001020018.1:p.Glu308Gln
NM_003242.5:c.847G>C	NP_003233.4:p.Glu283Gln
XM_011534043.1:c.874G>C	XP_011532345.1:p.Glu292Gln
XM_011534044.1:c.799G>C	XP_011532346.1:p.Glu267Gln
XM_011534045.1:c.742G>C	XP_011532347.1:p.Glu248Gln
XM_011534043.2:c.874G>C	XP_011532345.1:p.Glu292Gln
XM_011534045.3:c.742G>C	XP_011532347.1:p.Glu248Gln
XM_017007106.1:c.742G>C	XP_016862595.1:p.Glu248Gln
NM_003242.6:c.847G>C MANE Select	NP_003233.4:p.Glu283Gln