Canonical Allele Identifier: CA2336421208
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs2038067665

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342369del , CM000681.2:g.41342369del GRCh38
NC_000019.9:g.41848274del , CM000681.1:g.41848274del GRCh37
NC_000019.8:g.46540114del NCBI36
NG_013364.1:g.16558del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-122del MANE Select ENSP00000221930.4:n.635-122del
ENST00000600196.2:c.635-122del ENSP00000504008.1:n.635-122del
ENST00000677934.1:c.634+2378del ENSP00000504769.1:n.634+2378del
ENST00000221930.5:c.635-122del ENSP00000221930.4:n.635-122del
ENST00000597453.1:n.166-122del
ENST00000600196.1:n.95-122del
NM_000660.5:c.635-122del NP_000651.3:n.635-122del
XM_011527242.1:c.635-122del XP_011525544.1:n.635-122del
NM_000660.6:c.635-122del NP_000651.3:n.635-122del
XM_011527242.2:c.635-122del XP_011525544.1:n.635-122del
NM_000660.7:c.635-122del MANE Select NP_000651.3:n.635-122del