Canonical Allele Identifier: CA1584791114
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046572G= , CM000667.2:g.136046572G= GRCh38
NC_000005.9:g.135382261G= , CM000667.1:g.135382261G= GRCh37
NC_000005.8:g.135410160G= NCBI36
NG_012646.1:g.22678G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+77G= MANE Select ENSP00000416330.2:n.459+77G=
ENST00000442011.6:c.459+77G= ENSP00000416330.2:n.459+77G=
ENST00000506699.5:n.601G=
ENST00000507018.5:c.437+16G=
ENST00000515433.1:n.828G=
NM_000358.2:c.459+77G= NP_000349.1:n.459+77G=
NM_000358.3:c.459+77G= MANE Select NP_000349.1:n.459+77G=