Canonical Allele Identifier: CA2336416612
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs2037945251

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332541del , CM000681.2:g.41332541del GRCh38
NC_000019.9:g.41838446del , CM000681.1:g.41838446del GRCh37
NC_000019.8:g.46530286del NCBI36
NG_013364.1:g.26386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-260del MANE Select ENSP00000221930.4:n.861-260del
ENST00000600196.2:c.713-260del ENSP00000504008.1:n.713-260del
ENST00000677934.1:c.635-260del ENSP00000504769.1:n.635-260del
ENST00000221930.5:c.861-260del ENSP00000221930.4:n.861-260del
ENST00000598758.5:c.149-260del
ENST00000600196.1:n.173-260del
NM_000660.5:c.861-260del NP_000651.3:n.861-260del
XM_011527242.1:c.864-260del XP_011525544.1:n.864-260del
NM_000660.6:c.861-260del NP_000651.3:n.861-260del
XM_011527242.2:c.864-260del XP_011525544.1:n.864-260del
NM_000660.7:c.861-260del MANE Select NP_000651.3:n.861-260del