Canonical Allele Identifier: CA2336416607
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332536A= , CM000681.2:g.41332536A= GRCh38
NC_000019.9:g.41838441A= , CM000681.1:g.41838441A= GRCh37
NC_000019.8:g.46530281A= NCBI36
NG_013364.1:g.26391T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-255T= MANE Select ENSP00000221930.4:n.861-255T=
ENST00000600196.2:c.713-255T= ENSP00000504008.1:n.713-255T=
ENST00000677934.1:c.635-255T= ENSP00000504769.1:n.635-255T=
ENST00000221930.5:c.861-255T= ENSP00000221930.4:n.861-255T=
ENST00000598758.5:c.149-255T=
ENST00000600196.1:n.173-255T=
NM_000660.5:c.861-255T= NP_000651.3:n.861-255T=
XM_011527242.1:c.864-255T= XP_011525544.1:n.864-255T=
NM_000660.6:c.861-255T= NP_000651.3:n.861-255T=
XM_011527242.2:c.864-255T= XP_011525544.1:n.864-255T=
NM_000660.7:c.861-255T= MANE Select NP_000651.3:n.861-255T=