Canonical Allele Identifier: CA351807606

Gene: TGFBR2

Linked Data

• dbSNP Id: rs781692282
• MyVariant Identifiers: chr3:g.30713342G>C (hg19) ; chr3:g.30671850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671850G>C , CM000665.2:g.30671850G>C	GRCh38
NC_000003.11:g.30713342G>C , CM000665.1:g.30713342G>C	GRCh37
NC_000003.10:g.30688346G>C	NCBI36
NG_007490.1:g.70349G>C , LRG_779:g.70349G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.667G>C MANE Select	ENSP00000295754.5:p.Asp223His
ENST00000672866.1:n.2263G>C
ENST00000295754.9:c.667G>C	ENSP00000295754.5:p.Asp223His
ENST00000359013.4:c.742G>C	ENSP00000351905.4:p.Asp248His
NM_001024847.2:c.742G>C , LRG_779t1:c.742G>C	NP_001020018.1:p.Asp248His
NM_003242.5:c.667G>C	NP_003233.4:p.Asp223His
XM_011534043.1:c.694G>C	XP_011532345.1:p.Asp232His
XM_011534044.1:c.619G>C	XP_011532346.1:p.Asp207His
XM_011534045.1:c.562G>C	XP_011532347.1:p.Asp188His
XM_011534043.2:c.694G>C	XP_011532345.1:p.Asp232His
XM_011534045.3:c.562G>C	XP_011532347.1:p.Asp188His
XM_017007106.1:c.562G>C	XP_016862595.1:p.Asp188His
NM_003242.6:c.667G>C MANE Select	NP_003233.4:p.Asp223His