Canonical Allele Identifier: CA2336416561
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332420G= , CM000681.2:g.41332420G= GRCh38
NC_000019.9:g.41838325G= , CM000681.1:g.41838325G= GRCh37
NC_000019.8:g.46530165G= NCBI36
NG_013364.1:g.26507C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-139C= MANE Select ENSP00000221930.4:n.861-139C=
ENST00000600196.2:c.713-139C= ENSP00000504008.1:n.713-139C=
ENST00000677934.1:c.635-139C= ENSP00000504769.1:n.635-139C=
ENST00000221930.5:c.861-139C= ENSP00000221930.4:n.861-139C=
ENST00000598758.5:c.149-139C=
ENST00000600196.1:n.173-139C=
NM_000660.5:c.861-139C= NP_000651.3:n.861-139C=
XM_011527242.1:c.864-139C= XP_011525544.1:n.864-139C=
NM_000660.6:c.861-139C= NP_000651.3:n.861-139C=
XM_011527242.2:c.864-139C= XP_011525544.1:n.864-139C=
NM_000660.7:c.861-139C= MANE Select NP_000651.3:n.861-139C=