Canonical Allele Identifier: CA2336421035
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342037T= , CM000681.2:g.41342037T= GRCh38
NC_000019.9:g.41847942T= , CM000681.1:g.41847942T= GRCh37
NC_000019.8:g.46539782T= NCBI36
NG_013364.1:g.16890A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.713-7A= MANE Select ENSP00000221930.4:n.713-7A=
ENST00000600196.2:c.712+133A= ENSP00000504008.1:n.712+133A=
ENST00000677934.1:c.634+2710A= ENSP00000504769.1:n.634+2710A=
ENST00000221930.5:c.713-7A= ENSP00000221930.4:n.713-7A=
ENST00000597453.1:n.376A=
ENST00000600196.1:n.172+133A=
NM_000660.5:c.713-7A= NP_000651.3:n.713-7A=
XM_011527242.1:c.713-4A= XP_011525544.1:n.713-4A=
NM_000660.6:c.713-7A= NP_000651.3:n.713-7A=
XM_011527242.2:c.713-4A= XP_011525544.1:n.713-4A=
NM_000660.7:c.713-7A= MANE Select NP_000651.3:n.713-7A=