Canonical Allele Identifier: CA1584790993
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046332C= , CM000667.2:g.136046332C= GRCh38
NC_000005.9:g.135382021C= , CM000667.1:g.135382021C= GRCh37
NC_000005.8:g.135409920C= NCBI36
NG_012646.1:g.22438C=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-3C= MANE Select ENSP00000416330.2:n.299-3C=
ENST00000442011.6:c.299-3C= ENSP00000416330.2:n.299-3C=
ENST00000504185.5:n.456-3C=
ENST00000506699.5:n.364-3C=
ENST00000507018.5:c.216-3C=
ENST00000515433.1:n.588C=
NM_000358.2:c.299-3C= NP_000349.1:n.299-3C=
NM_000358.3:c.299-3C= MANE Select NP_000349.1:n.299-3C=
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