Canonical Allele Identifier: CA1354873897

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1699385557
• gnomAD v3: 3-30673932-TA-T
• gnomAD v4: 3-30673932-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30673938del , CM000665.2:g.30673938del	GRCh38
NC_000003.11:g.30715430del , CM000665.1:g.30715430del	GRCh37
NC_000003.10:g.30690434del	NCBI36
NG_007490.1:g.72437del , LRG_779:g.72437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1255-167del MANE Select	ENSP00000295754.5:n.1255-167del
ENST00000672866.1:n.2851-167del
ENST00000295754.9:c.1255-167del	ENSP00000295754.5:n.1255-167del
ENST00000359013.4:c.1330-167del	ENSP00000351905.4:n.1330-167del
NM_001024847.2:c.1330-167del , LRG_779t1:c.1330-167del	NP_001020018.1:n.1330-167del
NM_003242.5:c.1255-167del	NP_003233.4:n.1255-167del
XM_011534043.1:c.1282-167del	XP_011532345.1:n.1282-167del
XM_011534044.1:c.1207-167del	XP_011532346.1:n.1207-167del
XM_011534045.1:c.1150-167del	XP_011532347.1:n.1150-167del
XM_011534043.2:c.1282-167del	XP_011532345.1:n.1282-167del
XM_011534045.3:c.1150-167del	XP_011532347.1:n.1150-167del
XM_017007106.1:c.1150-167del	XP_016862595.1:n.1150-167del
NM_003242.6:c.1255-167del MANE Select	NP_003233.4:n.1255-167del