Canonical Allele Identifier: CA351808697

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125436744
• MyVariant Identifiers: chr3:g.30713850C>T (hg19) ; chr3:g.30672358C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672358C>T , CM000665.2:g.30672358C>T	GRCh38
NC_000003.11:g.30713850C>T , CM000665.1:g.30713850C>T	GRCh37
NC_000003.10:g.30688854C>T	NCBI36
NG_007490.1:g.70857C>T , LRG_779:g.70857C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1175C>T MANE Select	ENSP00000295754.5:p.Thr392Ile
ENST00000672866.1:n.2771C>T
ENST00000295754.9:c.1175C>T	ENSP00000295754.5:p.Thr392Ile
ENST00000359013.4:c.1250C>T	ENSP00000351905.4:p.Thr417Ile
NM_001024847.2:c.1250C>T , LRG_779t1:c.1250C>T	NP_001020018.1:p.Thr417Ile
NM_003242.5:c.1175C>T	NP_003233.4:p.Thr392Ile
XM_011534043.1:c.1202C>T	XP_011532345.1:p.Thr401Ile
XM_011534044.1:c.1127C>T	XP_011532346.1:p.Thr376Ile
XM_011534045.1:c.1070C>T	XP_011532347.1:p.Thr357Ile
XM_011534043.2:c.1202C>T	XP_011532345.1:p.Thr401Ile
XM_011534045.3:c.1070C>T	XP_011532347.1:p.Thr357Ile
XM_017007106.1:c.1070C>T	XP_016862595.1:p.Thr357Ile
NM_003242.6:c.1175C>T MANE Select	NP_003233.4:p.Thr392Ile