Canonical Allele Identifier: CA1584791032
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046417G= , CM000667.2:g.136046417G= GRCh38
NC_000005.9:g.135382106G= , CM000667.1:g.135382106G= GRCh37
NC_000005.8:g.135410005G= NCBI36
NG_012646.1:g.22523G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.381G= MANE Select ENSP00000416330.2:p.Lys127=
ENST00000442011.6:c.381G= ENSP00000416330.2:p.Lys127=
ENST00000504185.5:n.538G=
ENST00000506699.5:n.446G=
ENST00000507018.5:c.298G=
ENST00000515433.1:n.673G=
NM_000358.2:c.381G= NP_000349.1:p.Lys127=
NM_000358.3:c.381G= MANE Select NP_000349.1:p.Lys127=