Canonical Allele Identifier: CA1584790813
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136045963A= , CM000667.2:g.136045963A= GRCh38
NC_000005.9:g.135381652A= , CM000667.1:g.135381652A= GRCh37
NC_000005.8:g.135409551A= NCBI36
NG_012646.1:g.22069A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-372A= MANE Select ENSP00000416330.2:n.299-372A=
ENST00000442011.6:c.299-372A= ENSP00000416330.2:n.299-372A=
ENST00000504185.5:n.456-372A=
ENST00000506699.5:n.364-372A=
ENST00000507018.5:c.216-372A=
ENST00000515433.1:n.219A=
NM_000358.2:c.299-372A= NP_000349.1:n.299-372A=
NM_000358.3:c.299-372A= MANE Select NP_000349.1:n.299-372A=
Search 100 bp 5'
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