Canonical Allele Identifier: CA1584790901
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046178C= , CM000667.2:g.136046178C= GRCh38
NC_000005.9:g.135381867C= , CM000667.1:g.135381867C= GRCh37
NC_000005.8:g.135409766C= NCBI36
NG_012646.1:g.22284C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-157C= MANE Select ENSP00000416330.2:n.299-157C=
ENST00000442011.6:c.299-157C= ENSP00000416330.2:n.299-157C=
ENST00000504185.5:n.456-157C=
ENST00000506699.5:n.364-157C=
ENST00000507018.5:c.216-157C=
ENST00000515433.1:n.434C=
NM_000358.2:c.299-157C= NP_000349.1:n.299-157C=
NM_000358.3:c.299-157C= MANE Select NP_000349.1:n.299-157C=
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