Canonical Allele Identifier: CA2336420998
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341955G= , CM000681.2:g.41341955G= GRCh38
NC_000019.9:g.41847860G= , CM000681.1:g.41847860G= GRCh37
NC_000019.8:g.46539700G= NCBI36
NG_013364.1:g.16972C=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.788C= MANE Select NP_000651.3:p.Thr263=
ENST00000221930.6:c.788C= MANE Select ENSP00000221930.4:p.Thr263=
NM_000660.5:c.788C= NP_000651.3:p.Thr263=
NM_000660.6:c.788C= NP_000651.3:p.Thr263=
ENST00000221930.5:c.788C= ENSP00000221930.4:p.Thr263=
ENST00000598758.5:c.76C=
ENST00000600196.1:n.172+215C=
ENST00000600196.2:c.712+215C= ENSP00000504008.1:n.712+215C=
ENST00000677934.1:c.634+2792C= ENSP00000504769.1:n.634+2792C=
XM_011527242.1:c.791C= XP_011525544.1:p.Thr264=
XM_011527242.2:c.791C= XP_011525544.1:p.Thr264=