Canonical Allele Identifier: CA1584798678
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136057072G= , CM000667.2:g.136057072G= GRCh38
NC_000005.9:g.135392761G= , CM000667.1:g.135392761G= GRCh37
NC_000005.8:g.135420660G= NCBI36
NG_012646.1:g.33178G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1678+277G= MANE Select ENSP00000416330.2:n.1678+277G=
ENST00000442011.6:c.1678+277G= ENSP00000416330.2:n.1678+277G=
ENST00000506699.5:n.2195+277G=
ENST00000507018.5:c.1656+277G=
ENST00000509485.5:c.675+277G=
ENST00000514242.5:n.449+277G=
ENST00000514554.5:c.830+277G=
NM_000358.2:c.1678+277G= NP_000349.1:n.1678+277G=
NM_000358.3:c.1678+277G= MANE Select NP_000349.1:n.1678+277G=