Canonical Allele Identifier: CA2336421142
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342235C= , CM000681.2:g.41342235C= GRCh38
NC_000019.9:g.41848140C= , CM000681.1:g.41848140C= GRCh37
NC_000019.8:g.46539980C= NCBI36
NG_013364.1:g.16692G=

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.647G= MANE Select ENSP00000221930.4:p.Gly216=
ENST00000600196.2:c.647G= ENSP00000504008.1:p.Gly216=
ENST00000677934.1:c.634+2512G= ENSP00000504769.1:n.634+2512G=
ENST00000221930.5:c.647G= ENSP00000221930.4:p.Gly216=
ENST00000597453.1:n.178G=
ENST00000600196.1:n.107G=
NM_000660.5:c.647G= NP_000651.3:p.Gly216=
XM_011527242.1:c.647G= XP_011525544.1:p.Gly216=
NM_000660.6:c.647G= NP_000651.3:p.Gly216=
XM_011527242.2:c.647G= XP_011525544.1:p.Gly216=
NM_000660.7:c.647G= MANE Select NP_000651.3:p.Gly216=