Canonical Allele Identifier: CA1584798561
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056931G= , CM000667.2:g.136056931G= GRCh38
NC_000005.9:g.135392620G= , CM000667.1:g.135392620G= GRCh37
NC_000005.8:g.135420519G= NCBI36
NG_012646.1:g.33037G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1678+136G= MANE Select ENSP00000416330.2:n.1678+136G=
ENST00000442011.6:c.1678+136G= ENSP00000416330.2:n.1678+136G=
ENST00000506699.5:n.2195+136G=
ENST00000507018.5:c.1656+136G=
ENST00000509485.5:c.675+136G=
ENST00000514242.5:n.449+136G=
ENST00000514554.5:c.830+136G=
NM_000358.2:c.1678+136G= NP_000349.1:n.1678+136G=
NM_000358.3:c.1678+136G= MANE Select NP_000349.1:n.1678+136G=
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