Canonical Allele Identifier: CA1584790898
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046170A= , CM000667.2:g.136046170A= GRCh38
NC_000005.9:g.135381859A= , CM000667.1:g.135381859A= GRCh37
NC_000005.8:g.135409758A= NCBI36
NG_012646.1:g.22276A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-165A= MANE Select ENSP00000416330.2:n.299-165A=
ENST00000442011.6:c.299-165A= ENSP00000416330.2:n.299-165A=
ENST00000504185.5:n.456-165A=
ENST00000506699.5:n.364-165A=
ENST00000507018.5:c.216-165A=
ENST00000515433.1:n.426A=
NM_000358.2:c.299-165A= NP_000349.1:n.299-165A=
NM_000358.3:c.299-165A= MANE Select NP_000349.1:n.299-165A=
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