Canonical Allele Identifier: CA2336416598
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332518T= , CM000681.2:g.41332518T= GRCh38
NC_000019.9:g.41838423T= , CM000681.1:g.41838423T= GRCh37
NC_000019.8:g.46530263T= NCBI36
NG_013364.1:g.26409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-237A= MANE Select ENSP00000221930.4:n.861-237A=
ENST00000600196.2:c.713-237A= ENSP00000504008.1:n.713-237A=
ENST00000677934.1:c.635-237A= ENSP00000504769.1:n.635-237A=
ENST00000221930.5:c.861-237A= ENSP00000221930.4:n.861-237A=
ENST00000598758.5:c.149-237A=
ENST00000600196.1:n.173-237A=
NM_000660.5:c.861-237A= NP_000651.3:n.861-237A=
XM_011527242.1:c.864-237A= XP_011525544.1:n.864-237A=
NM_000660.6:c.861-237A= NP_000651.3:n.861-237A=
XM_011527242.2:c.864-237A= XP_011525544.1:n.864-237A=
NM_000660.7:c.861-237A= MANE Select NP_000651.3:n.861-237A=