Canonical Allele Identifier: CA1584791153
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046637G= , CM000667.2:g.136046637G= GRCh38
NC_000005.9:g.135382326G= , CM000667.1:g.135382326G= GRCh37
NC_000005.8:g.135410225G= NCBI36
NG_012646.1:g.22743G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+142G= MANE Select ENSP00000416330.2:n.459+142G=
ENST00000442011.6:c.459+142G= ENSP00000416330.2:n.459+142G=
ENST00000506699.5:n.666G=
ENST00000507018.5:c.437+81G=
ENST00000515433.1:n.893G=
NM_000358.2:c.459+142G= NP_000349.1:n.459+142G=
NM_000358.3:c.459+142G= MANE Select NP_000349.1:n.459+142G=