Canonical Allele Identifier: CA1584790979
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046313C= , CM000667.2:g.136046313C= GRCh38
NC_000005.9:g.135382002C= , CM000667.1:g.135382002C= GRCh37
NC_000005.8:g.135409901C= NCBI36
NG_012646.1:g.22419C=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-22C= MANE Select ENSP00000416330.2:n.299-22C=
ENST00000442011.6:c.299-22C= ENSP00000416330.2:n.299-22C=
ENST00000504185.5:n.456-22C=
ENST00000506699.5:n.364-22C=
ENST00000507018.5:c.216-22C=
ENST00000515433.1:n.569C=
NM_000358.2:c.299-22C= NP_000349.1:n.299-22C=
NM_000358.3:c.299-22C= MANE Select NP_000349.1:n.299-22C=
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