Canonical Allele Identifier: CA2336416468
Community Standard Title: NM_000660.7(TGFB1):c.897C= (p.Tyr299=)
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332245G= , CM000681.2:g.41332245G= GRCh38
NC_000019.9:g.41838150G= , CM000681.1:g.41838150G= GRCh37
NC_000019.8:g.46529990G= NCBI36
NG_013364.1:g.26682C=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.897C= MANE Select NP_000651.3:p.Tyr299=
ENST00000221930.6:c.897C= MANE Select ENSP00000221930.4:p.Tyr299=
NM_000660.5:c.897C= NP_000651.3:p.Tyr299=
NM_000660.6:c.897C= NP_000651.3:p.Tyr299=
ENST00000221930.5:c.897C= ENSP00000221930.4:p.Tyr299=
ENST00000598758.5:c.185C=
ENST00000600196.1:n.209C=
ENST00000600196.2:c.749C= ENSP00000504008.1:p.Thr250=
ENST00000677934.1:c.671C= ENSP00000504769.1:p.Thr224=
XM_011527242.1:c.900C= XP_011525544.1:p.Tyr300=
XM_011527242.2:c.900C= XP_011525544.1:p.Tyr300=