Canonical Allele Identifier: CA2336421138
Community Standard Title: NM_000660.7(TGFB1):c.653G= (p.Arg218=)
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342229C= , CM000681.2:g.41342229C= GRCh38
NC_000019.9:g.41848134C= , CM000681.1:g.41848134C= GRCh37
NC_000019.8:g.46539974C= NCBI36
NG_013364.1:g.16698G=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.653G= MANE Select NP_000651.3:p.Arg218=
ENST00000221930.6:c.653G= MANE Select ENSP00000221930.4:p.Arg218=
NM_000660.5:c.653G= NP_000651.3:p.Arg218=
NM_000660.6:c.653G= NP_000651.3:p.Arg218=
ENST00000221930.5:c.653G= ENSP00000221930.4:p.Arg218=
ENST00000597453.1:n.184G=
ENST00000600196.1:n.113G=
ENST00000600196.2:c.653G= ENSP00000504008.1:p.Arg218=
ENST00000677934.1:c.634+2518G= ENSP00000504769.1:n.634+2518G=
XM_011527242.1:c.653G= XP_011525544.1:p.Arg218=
XM_011527242.2:c.653G= XP_011525544.1:p.Arg218=