Canonical Allele Identifier: CA1584791163
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046671G= , CM000667.2:g.136046671G= GRCh38
NC_000005.9:g.135382360G= , CM000667.1:g.135382360G= GRCh37
NC_000005.8:g.135410259G= NCBI36
NG_012646.1:g.22777G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+176G= MANE Select ENSP00000416330.2:n.459+176G=
ENST00000442011.6:c.459+176G= ENSP00000416330.2:n.459+176G=
ENST00000506699.5:n.700G=
ENST00000507018.5:c.437+115G=
ENST00000515433.1:n.927G=
NM_000358.2:c.459+176G= NP_000349.1:n.459+176G=
NM_000358.3:c.459+176G= MANE Select NP_000349.1:n.459+176G=
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