Canonical Allele Identifier: CA2336418792
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41337563T= , CM000681.2:g.41337563T= GRCh38
NC_000019.9:g.41843468T= , CM000681.1:g.41843468T= GRCh37
NC_000019.8:g.46535308T= NCBI36
NG_013364.1:g.21364A=

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.860+4320A= MANE Select ENSP00000221930.4:n.860+4320A=
ENST00000600196.2:c.712+4607A= ENSP00000504008.1:n.712+4607A=
ENST00000677934.1:c.635-5282A= ENSP00000504769.1:n.635-5282A=
ENST00000221930.5:c.860+4320A= ENSP00000221930.4:n.860+4320A=
ENST00000598758.5:c.148+4320A=
ENST00000600196.1:n.172+4607A=
NM_000660.5:c.860+4320A= NP_000651.3:n.860+4320A=
XM_011527242.1:c.863+4320A= XP_011525544.1:n.863+4320A=
NM_000660.6:c.860+4320A= NP_000651.3:n.860+4320A=
XM_011527242.2:c.863+4320A= XP_011525544.1:n.863+4320A=
NM_000660.7:c.860+4320A= MANE Select NP_000651.3:n.860+4320A=