Canonical Allele Identifier: CA2336420987
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341925C= , CM000681.2:g.41341925C= GRCh38
NC_000019.9:g.41847830C= , CM000681.1:g.41847830C= GRCh37
NC_000019.8:g.46539670C= NCBI36
NG_013364.1:g.17002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.818G= MANE Select ENSP00000221930.4:p.Ser273=
ENST00000600196.2:c.712+245G= ENSP00000504008.1:n.712+245G=
ENST00000677934.1:c.634+2822G= ENSP00000504769.1:n.634+2822G=
ENST00000221930.5:c.818G= ENSP00000221930.4:p.Ser273=
ENST00000598758.5:c.106G=
ENST00000600196.1:n.172+245G=
NM_000660.5:c.818G= NP_000651.3:p.Ser273=
XM_011527242.1:c.821G= XP_011525544.1:p.Ser274=
NM_000660.6:c.818G= NP_000651.3:p.Ser273=
XM_011527242.2:c.821G= XP_011525544.1:p.Ser274=
NM_000660.7:c.818G= MANE Select NP_000651.3:p.Ser273=