Canonical Allele Identifier: CA2336416464
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332236G= , CM000681.2:g.41332236G= GRCh38
NC_000019.9:g.41838141G= , CM000681.1:g.41838141G= GRCh37
NC_000019.8:g.46529981G= NCBI36
NG_013364.1:g.26691C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.906C= MANE Select ENSP00000221930.4:p.Phe302=
ENST00000600196.2:c.758C= ENSP00000504008.1:p.Ser253=
ENST00000677934.1:c.680C= ENSP00000504769.1:p.Ser227=
ENST00000221930.5:c.906C= ENSP00000221930.4:p.Phe302=
ENST00000598758.5:c.194C=
ENST00000600196.1:n.218C=
NM_000660.5:c.906C= NP_000651.3:p.Phe302=
XM_011527242.1:c.909C= XP_011525544.1:p.Phe303=
NM_000660.6:c.906C= NP_000651.3:p.Phe302=
XM_011527242.2:c.909C= XP_011525544.1:p.Phe303=
NM_000660.7:c.906C= MANE Select NP_000651.3:p.Phe302=