Canonical Allele Identifier: CA2336420961
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341862C= , CM000681.2:g.41341862C= GRCh38
NC_000019.9:g.41847767C= , CM000681.1:g.41847767C= GRCh37
NC_000019.8:g.46539607C= NCBI36
NG_013364.1:g.17065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.860+21G= MANE Select ENSP00000221930.4:n.860+21G=
ENST00000600196.2:c.712+308G= ENSP00000504008.1:n.712+308G=
ENST00000677934.1:c.634+2885G= ENSP00000504769.1:n.634+2885G=
ENST00000221930.5:c.860+21G= ENSP00000221930.4:n.860+21G=
ENST00000598758.5:c.148+21G=
ENST00000600196.1:n.172+308G=
NM_000660.5:c.860+21G= NP_000651.3:n.860+21G=
XM_011527242.1:c.863+21G= XP_011525544.1:n.863+21G=
NM_000660.6:c.860+21G= NP_000651.3:n.860+21G=
XM_011527242.2:c.863+21G= XP_011525544.1:n.863+21G=
NM_000660.7:c.860+21G= MANE Select NP_000651.3:n.860+21G=