Canonical Allele Identifier: CA995955771

Gene: TGFB1

Linked Data

• dbSNP Id: rs2038068482
• gnomAD v3: 19-41342407-TTTTTTTG-T
• gnomAD v4: 19-41342407-TTTTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342408_41342414del , CM000681.2:g.41342408_41342414del	GRCh38
NC_000019.9:g.41848313_41848319del , CM000681.1:g.41848313_41848319del	GRCh37
NC_000019.8:g.46540153_46540159del	NCBI36
NG_013364.1:g.16513_16519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-167_635-161del MANE Select	ENSP00000221930.4:n.635-167_635-161del
ENST00000600196.2:c.635-167_635-161del	ENSP00000504008.1:n.635-167_635-161del
ENST00000677934.1:c.634+2333_634+2339del	ENSP00000504769.1:n.634+2333_634+2339del
ENST00000221930.5:c.635-167_635-161del	ENSP00000221930.4:n.635-167_635-161del
ENST00000597453.1:n.166-167_166-161del
ENST00000600196.1:n.95-167_95-161del
NM_000660.5:c.635-167_635-161del	NP_000651.3:n.635-167_635-161del
XM_011527242.1:c.635-167_635-161del	XP_011525544.1:n.635-167_635-161del
NM_000660.6:c.635-167_635-161del	NP_000651.3:n.635-167_635-161del
XM_011527242.2:c.635-167_635-161del	XP_011525544.1:n.635-167_635-161del
NM_000660.7:c.635-167_635-161del MANE Select	NP_000651.3:n.635-167_635-161del