Canonical Allele Identifier: CA2336418786
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41337556T= , CM000681.2:g.41337556T= GRCh38
NC_000019.9:g.41843461T= , CM000681.1:g.41843461T= GRCh37
NC_000019.8:g.46535301T= NCBI36
NG_013364.1:g.21371A=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.860+4327A= MANE Select NP_000651.3:n.860+4327A=
ENST00000221930.6:c.860+4327A= MANE Select ENSP00000221930.4:n.860+4327A=
NM_000660.5:c.860+4327A= NP_000651.3:n.860+4327A=
NM_000660.6:c.860+4327A= NP_000651.3:n.860+4327A=
ENST00000221930.5:c.860+4327A= ENSP00000221930.4:n.860+4327A=
ENST00000598758.5:c.148+4327A=
ENST00000600196.1:n.172+4614A=
ENST00000600196.2:c.712+4614A= ENSP00000504008.1:n.712+4614A=
ENST00000677934.1:c.635-5275A= ENSP00000504769.1:n.635-5275A=
XM_011527242.1:c.863+4327A= XP_011525544.1:n.863+4327A=
XM_011527242.2:c.863+4327A= XP_011525544.1:n.863+4327A=