Canonical Allele Identifier: CA2336420051
Community Standard Title: NM_000660.7(TGFB1):c.860+1916T=
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41339967A= , CM000681.2:g.41339967A= GRCh38
NC_000019.9:g.41845872A= , CM000681.1:g.41845872A= GRCh37
NC_000019.8:g.46537712A= NCBI36
NG_013364.1:g.18960T=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.860+1916T= MANE Select NP_000651.3:n.860+1916T=
ENST00000221930.6:c.860+1916T= MANE Select ENSP00000221930.4:n.860+1916T=
NM_000660.5:c.860+1916T= NP_000651.3:n.860+1916T=
NM_000660.6:c.860+1916T= NP_000651.3:n.860+1916T=
ENST00000221930.5:c.860+1916T= ENSP00000221930.4:n.860+1916T=
ENST00000598758.5:c.148+1916T=
ENST00000600196.1:n.172+2203T=
ENST00000600196.2:c.712+2203T= ENSP00000504008.1:n.712+2203T=
ENST00000677934.1:c.634+4780T= ENSP00000504769.1:n.634+4780T=
XM_011527242.1:c.863+1916T= XP_011525544.1:n.863+1916T=
XM_011527242.2:c.863+1916T= XP_011525544.1:n.863+1916T=