Canonical Allele Identifier: CA2336421134
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342222G= , CM000681.2:g.41342222G= GRCh38
NC_000019.9:g.41848127G= , CM000681.1:g.41848127G= GRCh37
NC_000019.8:g.46539967G= NCBI36
NG_013364.1:g.16705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.660C= MANE Select ENSP00000221930.4:p.Ser220=
ENST00000600196.2:c.660C= ENSP00000504008.1:p.Ser220=
ENST00000677934.1:c.634+2525C= ENSP00000504769.1:n.634+2525C=
ENST00000221930.5:c.660C= ENSP00000221930.4:p.Ser220=
ENST00000597453.1:n.191C=
ENST00000600196.1:n.120C=
NM_000660.5:c.660C= NP_000651.3:p.Ser220=
XM_011527242.1:c.660C= XP_011525544.1:p.Ser220=
NM_000660.6:c.660C= NP_000651.3:p.Ser220=
XM_011527242.2:c.660C= XP_011525544.1:p.Ser220=
NM_000660.7:c.660C= MANE Select NP_000651.3:p.Ser220=