Canonical Allele Identifier: CA020567

Gene: TGFBR2

Linked Data

• ClinVar Variation Id: 43688
• ClinVar RCV Id: RCV000036638
• dbSNP Id: rs397516492
• MyVariant Identifiers: chr3:g.30713662C>T (hg19) ; chr3:g.30672170C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672170C>T , CM000665.2:g.30672170C>T	GRCh38
NC_000003.11:g.30713662C>T , CM000665.1:g.30713662C>T	GRCh37
NC_000003.10:g.30688666C>T	NCBI36
NG_007490.1:g.70669C>T , LRG_779:g.70669C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.987C>T MANE Select	ENSP00000295754.5:p.Ala329=
ENST00000672866.1:n.2583C>T
ENST00000295754.9:c.987C>T	ENSP00000295754.5:p.Ala329=
ENST00000359013.4:c.1062C>T	ENSP00000351905.4:p.Ala354=
NM_001024847.2:c.1062C>T , LRG_779t1:c.1062C>T	NP_001020018.1:p.Ala354=
NM_003242.5:c.987C>T	NP_003233.4:p.Ala329=
XM_011534043.1:c.1014C>T	XP_011532345.1:p.Ala338=
XM_011534044.1:c.939C>T	XP_011532346.1:p.Ala313=
XM_011534045.1:c.882C>T	XP_011532347.1:p.Ala294=
XM_011534043.2:c.1014C>T	XP_011532345.1:p.Ala338=
XM_011534045.3:c.882C>T	XP_011532347.1:p.Ala294=
XM_017007106.1:c.882C>T	XP_016862595.1:p.Ala294=
NM_003242.6:c.987C>T MANE Select	NP_003233.4:p.Ala329=