Canonical Allele Identifier: CA433058966

Gene: TGFBR2

Linked Data

• ClinVar Variation Id: 700373
• ClinVar RCV Id: RCV000868519 ; RCV001552006 ; RCV004003022
• dbSNP Id: rs1575157891
• gnomAD v4: 3-30672161-C-T
• MyVariant Identifiers: chr3:g.30713653C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672161C>T , CM000665.2:g.30672161C>T	GRCh38
NC_000003.11:g.30713653C>T , CM000665.1:g.30713653C>T	GRCh37
NC_000003.10:g.30688657C>T	NCBI36
NG_007490.1:g.70660C>T , LRG_779:g.70660C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.978C>T MANE Select	ENSP00000295754.5:p.Ala326=
ENST00000672866.1:n.2574C>T
ENST00000295754.9:c.978C>T	ENSP00000295754.5:p.Ala326=
ENST00000359013.4:c.1053C>T	ENSP00000351905.4:p.Ala351=
NM_001024847.2:c.1053C>T , LRG_779t1:c.1053C>T	NP_001020018.1:p.Ala351=
NM_003242.5:c.978C>T	NP_003233.4:p.Ala326=
XM_011534043.1:c.1005C>T	XP_011532345.1:p.Ala335=
XM_011534044.1:c.930C>T	XP_011532346.1:p.Ala310=
XM_011534045.1:c.873C>T	XP_011532347.1:p.Ala291=
XM_011534043.2:c.1005C>T	XP_011532345.1:p.Ala335=
XM_011534045.3:c.873C>T	XP_011532347.1:p.Ala291=
XM_017007106.1:c.873C>T	XP_016862595.1:p.Ala291=
NM_003242.6:c.978C>T MANE Select	NP_003233.4:p.Ala326=