Canonical Allele Identifier: CA2336421256
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342423T= , CM000681.2:g.41342423T= GRCh38
NC_000019.9:g.41848328T= , CM000681.1:g.41848328T= GRCh37
NC_000019.8:g.46540168T= NCBI36
NG_013364.1:g.16504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-176A= MANE Select ENSP00000221930.4:n.635-176A=
ENST00000600196.2:c.635-176A= ENSP00000504008.1:n.635-176A=
ENST00000677934.1:c.634+2324A= ENSP00000504769.1:n.634+2324A=
ENST00000221930.5:c.635-176A= ENSP00000221930.4:n.635-176A=
ENST00000597453.1:n.166-176A=
ENST00000600196.1:n.95-176A=
NM_000660.5:c.635-176A= NP_000651.3:n.635-176A=
XM_011527242.1:c.635-176A= XP_011525544.1:n.635-176A=
NM_000660.6:c.635-176A= NP_000651.3:n.635-176A=
XM_011527242.2:c.635-176A= XP_011525544.1:n.635-176A=
NM_000660.7:c.635-176A= MANE Select NP_000651.3:n.635-176A=