Canonical Allele Identifier: CA1584790834
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046024T= , CM000667.2:g.136046024T= GRCh38
NC_000005.9:g.135381713T= , CM000667.1:g.135381713T= GRCh37
NC_000005.8:g.135409612T= NCBI36
NG_012646.1:g.22130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-311T= MANE Select ENSP00000416330.2:n.299-311T=
ENST00000442011.6:c.299-311T= ENSP00000416330.2:n.299-311T=
ENST00000504185.5:n.456-311T=
ENST00000506699.5:n.364-311T=
ENST00000507018.5:c.216-311T=
ENST00000515433.1:n.280T=
NM_000358.2:c.299-311T= NP_000349.1:n.299-311T=
NM_000358.3:c.299-311T= MANE Select NP_000349.1:n.299-311T=
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