Canonical Allele Identifier: CA2336420965
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341872A= , CM000681.2:g.41341872A= GRCh38
NC_000019.9:g.41847777A= , CM000681.1:g.41847777A= GRCh37
NC_000019.8:g.46539617A= NCBI36
NG_013364.1:g.17055T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.860+11T= MANE Select ENSP00000221930.4:n.860+11T=
ENST00000600196.2:c.712+298T= ENSP00000504008.1:n.712+298T=
ENST00000677934.1:c.634+2875T= ENSP00000504769.1:n.634+2875T=
ENST00000221930.5:c.860+11T= ENSP00000221930.4:n.860+11T=
ENST00000598758.5:c.148+11T=
ENST00000600196.1:n.172+298T=
NM_000660.5:c.860+11T= NP_000651.3:n.860+11T=
XM_011527242.1:c.863+11T= XP_011525544.1:n.863+11T=
NM_000660.6:c.860+11T= NP_000651.3:n.860+11T=
XM_011527242.2:c.863+11T= XP_011525544.1:n.863+11T=
NM_000660.7:c.860+11T= MANE Select NP_000651.3:n.860+11T=