Canonical Allele Identifier: CA351807616

Gene: TGFBR2

Linked Data

• ClinVar Variation Id: 1909964
• ClinVar RCV Id: RCV002600578
• dbSNP Id: rs112465572
• MyVariant Identifiers: chr3:g.30713346G>T (hg19) ; chr3:g.30671854G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671854G>T , CM000665.2:g.30671854G>T	GRCh38
NC_000003.11:g.30713346G>T , CM000665.1:g.30713346G>T	GRCh37
NC_000003.10:g.30688350G>T	NCBI36
NG_007490.1:g.70353G>T , LRG_779:g.70353G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.671G>T MANE Select	ENSP00000295754.5:p.Arg224Leu
ENST00000672866.1:n.2267G>T
ENST00000295754.9:c.671G>T	ENSP00000295754.5:p.Arg224Leu
ENST00000359013.4:c.746G>T	ENSP00000351905.4:p.Arg249Leu
NM_001024847.2:c.746G>T , LRG_779t1:c.746G>T	NP_001020018.1:p.Arg249Leu
NM_003242.5:c.671G>T	NP_003233.4:p.Arg224Leu
XM_011534043.1:c.698G>T	XP_011532345.1:p.Arg233Leu
XM_011534044.1:c.623G>T	XP_011532346.1:p.Arg208Leu
XM_011534045.1:c.566G>T	XP_011532347.1:p.Arg189Leu
XM_011534043.2:c.698G>T	XP_011532345.1:p.Arg233Leu
XM_011534045.3:c.566G>T	XP_011532347.1:p.Arg189Leu
XM_017007106.1:c.566G>T	XP_016862595.1:p.Arg189Leu
NM_003242.6:c.671G>T MANE Select	NP_003233.4:p.Arg224Leu