Canonical Allele Identifier: CA2336421191
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342345T= , CM000681.2:g.41342345T= GRCh38
NC_000019.9:g.41848250T= , CM000681.1:g.41848250T= GRCh37
NC_000019.8:g.46540090T= NCBI36
NG_013364.1:g.16582A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-98A= MANE Select ENSP00000221930.4:n.635-98A=
ENST00000600196.2:c.635-98A= ENSP00000504008.1:n.635-98A=
ENST00000677934.1:c.634+2402A= ENSP00000504769.1:n.634+2402A=
ENST00000221930.5:c.635-98A= ENSP00000221930.4:n.635-98A=
ENST00000597453.1:n.166-98A=
ENST00000600196.1:n.95-98A=
NM_000660.5:c.635-98A= NP_000651.3:n.635-98A=
XM_011527242.1:c.635-98A= XP_011525544.1:n.635-98A=
NM_000660.6:c.635-98A= NP_000651.3:n.635-98A=
XM_011527242.2:c.635-98A= XP_011525544.1:n.635-98A=
NM_000660.7:c.635-98A= MANE Select NP_000651.3:n.635-98A=