Canonical Allele Identifier: CA1584791138
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046616T= , CM000667.2:g.136046616T= GRCh38
NC_000005.9:g.135382305T= , CM000667.1:g.135382305T= GRCh37
NC_000005.8:g.135410204T= NCBI36
NG_012646.1:g.22722T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+121T= MANE Select ENSP00000416330.2:n.459+121T=
ENST00000442011.6:c.459+121T= ENSP00000416330.2:n.459+121T=
ENST00000506699.5:n.645T=
ENST00000507018.5:c.437+60T=
ENST00000515433.1:n.872T=
NM_000358.2:c.459+121T= NP_000349.1:n.459+121T=
NM_000358.3:c.459+121T= MANE Select NP_000349.1:n.459+121T=