Canonical Allele Identifier: CA71520729

Gene: TGFBR2

Linked Data

• dbSNP Id: rs942380119
• MyVariant Identifiers: chr3:g.30710214C>G (hg19) ; chr3:g.30668722C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30668722C>G , CM000665.2:g.30668722C>G	GRCh38
NC_000003.11:g.30710214C>G , CM000665.1:g.30710214C>G	GRCh37
NC_000003.10:g.30685218C>G	NCBI36
NG_007490.1:g.67221C>G , LRG_779:g.67221C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.455-2916C>G MANE Select	ENSP00000295754.5:n.455-2916C>G
ENST00000672866.1:n.2051-2916C>G
ENST00000295754.9:c.455-2916C>G	ENSP00000295754.5:n.455-2916C>G
ENST00000359013.4:c.530-2916C>G	ENSP00000351905.4:n.530-2916C>G
NM_001024847.2:c.530-2916C>G , LRG_779t1:c.530-2916C>G	NP_001020018.1:n.530-2916C>G
NM_003242.5:c.455-2916C>G	NP_003233.4:n.455-2916C>G
XM_011534043.1:c.482-2916C>G	XP_011532345.1:n.482-2916C>G
XM_011534044.1:c.407-2916C>G	XP_011532346.1:n.407-2916C>G
XM_011534045.1:c.350-2916C>G	XP_011532347.1:n.350-2916C>G
XM_011534043.2:c.482-2916C>G	XP_011532345.1:n.482-2916C>G
XM_011534045.3:c.350-2916C>G	XP_011532347.1:n.350-2916C>G
XM_017007106.1:c.350-2916C>G	XP_016862595.1:n.350-2916C>G
NM_003242.6:c.455-2916C>G MANE Select	NP_003233.4:n.455-2916C>G