Canonical Allele Identifier: CA1584791129
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046600C= , CM000667.2:g.136046600C= GRCh38
NC_000005.9:g.135382289C= , CM000667.1:g.135382289C= GRCh37
NC_000005.8:g.135410188C= NCBI36
NG_012646.1:g.22706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+105C= MANE Select ENSP00000416330.2:n.459+105C=
ENST00000442011.6:c.459+105C= ENSP00000416330.2:n.459+105C=
ENST00000506699.5:n.629C=
ENST00000507018.5:c.437+44C=
ENST00000515433.1:n.856C=
NM_000358.2:c.459+105C= NP_000349.1:n.459+105C=
NM_000358.3:c.459+105C= MANE Select NP_000349.1:n.459+105C=