Canonical Allele Identifier: CA351809142

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30715723T>G (hg19) ; chr3:g.30674231T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674231T>G , CM000665.2:g.30674231T>G	GRCh38
NC_000003.11:g.30715723T>G , CM000665.1:g.30715723T>G	GRCh37
NC_000003.10:g.30690727T>G	NCBI36
NG_007490.1:g.72730T>G , LRG_779:g.72730T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1381T>G MANE Select	ENSP00000295754.5:p.Cys461Gly
ENST00000672866.1:n.2977T>G
ENST00000673203.1:n.259T>G
ENST00000295754.9:c.1381T>G	ENSP00000295754.5:p.Cys461Gly
ENST00000359013.4:c.1456T>G	ENSP00000351905.4:p.Cys486Gly
NM_001024847.2:c.1456T>G , LRG_779t1:c.1456T>G	NP_001020018.1:p.Cys486Gly
NM_003242.5:c.1381T>G	NP_003233.4:p.Cys461Gly
XM_011534043.1:c.1408T>G	XP_011532345.1:p.Cys470Gly
XM_011534044.1:c.1333T>G	XP_011532346.1:p.Cys445Gly
XM_011534045.1:c.1276T>G	XP_011532347.1:p.Cys426Gly
XM_011534043.2:c.1408T>G	XP_011532345.1:p.Cys470Gly
XM_011534045.3:c.1276T>G	XP_011532347.1:p.Cys426Gly
XM_017007106.1:c.1276T>G	XP_016862595.1:p.Cys426Gly
NM_003242.6:c.1381T>G MANE Select	NP_003233.4:p.Cys461Gly