Canonical Allele Identifier: CA2336420990
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341933A= , CM000681.2:g.41341933A= GRCh38
NC_000019.9:g.41847838A= , CM000681.1:g.41847838A= GRCh37
NC_000019.8:g.46539678A= NCBI36
NG_013364.1:g.16994T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.810T= MANE Select ENSP00000221930.4:p.His270=
ENST00000600196.2:c.712+237T= ENSP00000504008.1:n.712+237T=
ENST00000677934.1:c.634+2814T= ENSP00000504769.1:n.634+2814T=
ENST00000221930.5:c.810T= ENSP00000221930.4:p.His270=
ENST00000598758.5:c.98T=
ENST00000600196.1:n.172+237T=
NM_000660.5:c.810T= NP_000651.3:p.His270=
XM_011527242.1:c.813T= XP_011525544.1:p.His271=
NM_000660.6:c.810T= NP_000651.3:p.His270=
XM_011527242.2:c.813T= XP_011525544.1:p.His271=
NM_000660.7:c.810T= MANE Select NP_000651.3:p.His270=