Canonical Allele Identifier: CA351807939

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1415684178
• MyVariant Identifiers: chr3:g.30713493C>A (hg19) ; chr3:g.30672001C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672001C>A , CM000665.2:g.30672001C>A	GRCh38
NC_000003.11:g.30713493C>A , CM000665.1:g.30713493C>A	GRCh37
NC_000003.10:g.30688497C>A	NCBI36
NG_007490.1:g.70500C>A , LRG_779:g.70500C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.818C>A MANE Select	ENSP00000295754.5:p.Thr273Lys
ENST00000672866.1:n.2414C>A
ENST00000295754.9:c.818C>A	ENSP00000295754.5:p.Thr273Lys
ENST00000359013.4:c.893C>A	ENSP00000351905.4:p.Thr298Lys
NM_001024847.2:c.893C>A , LRG_779t1:c.893C>A	NP_001020018.1:p.Thr298Lys
NM_003242.5:c.818C>A	NP_003233.4:p.Thr273Lys
XM_011534043.1:c.845C>A	XP_011532345.1:p.Thr282Lys
XM_011534044.1:c.770C>A	XP_011532346.1:p.Thr257Lys
XM_011534045.1:c.713C>A	XP_011532347.1:p.Thr238Lys
XM_011534043.2:c.845C>A	XP_011532345.1:p.Thr282Lys
XM_011534045.3:c.713C>A	XP_011532347.1:p.Thr238Lys
XM_017007106.1:c.713C>A	XP_016862595.1:p.Thr238Lys
NM_003242.6:c.818C>A MANE Select	NP_003233.4:p.Thr273Lys