Canonical Allele Identifier: CA2336421029
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342028A= , CM000681.2:g.41342028A= GRCh38
NC_000019.9:g.41847933A= , CM000681.1:g.41847933A= GRCh37
NC_000019.8:g.46539773A= NCBI36
NG_013364.1:g.16899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.715T= MANE Select ENSP00000221930.4:p.Phe239=
ENST00000600196.2:c.712+142T= ENSP00000504008.1:n.712+142T=
ENST00000677934.1:c.634+2719T= ENSP00000504769.1:n.634+2719T=
ENST00000221930.5:c.715T= ENSP00000221930.4:p.Phe239=
ENST00000597453.1:n.385T=
ENST00000598758.5:c.3T=
ENST00000600196.1:n.172+142T=
NM_000660.5:c.715T= NP_000651.3:p.Phe239=
XM_011527242.1:c.718T= XP_011525544.1:p.Phe240=
NM_000660.6:c.715T= NP_000651.3:p.Phe239=
XM_011527242.2:c.718T= XP_011525544.1:p.Phe240=
NM_000660.7:c.715T= MANE Select NP_000651.3:p.Phe239=