Canonical Allele Identifier: CA2336422652
Community Standard Title: NM_000660.7(TGFB1):c.517-740G=
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41345604C= , CM000681.2:g.41345604C= GRCh38
NC_000019.9:g.41851509C= , CM000681.1:g.41851509C= GRCh37
NC_000019.8:g.46543349C= NCBI36
NG_013364.1:g.13323G=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.517-740G= MANE Select NP_000651.3:n.517-740G=
ENST00000221930.6:c.517-740G= MANE Select ENSP00000221930.4:n.517-740G=
NM_000660.5:c.517-740G= NP_000651.3:n.517-740G=
NM_000660.6:c.517-740G= NP_000651.3:n.517-740G=
ENST00000221930.5:c.517-740G= ENSP00000221930.4:n.517-740G=
ENST00000597453.1:n.48-740G=
ENST00000600196.2:c.517-740G= ENSP00000504008.1:n.517-740G=
ENST00000677934.1:c.517-740G= ENSP00000504769.1:n.517-740G=
XM_011527242.1:c.517-740G= XP_011525544.1:n.517-740G=
XM_011527242.2:c.517-740G= XP_011525544.1:n.517-740G=