Canonical Allele Identifier: CA1584796803
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055589A= , CM000667.2:g.136055589A= GRCh38
NC_000005.9:g.135391278A= , CM000667.1:g.135391278A= GRCh37
NC_000005.8:g.135419177A= NCBI36
NG_012646.1:g.31695A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1411-91A= MANE Select ENSP00000416330.2:n.1411-91A=
ENST00000442011.6:c.1411-91A= ENSP00000416330.2:n.1411-91A=
ENST00000506699.5:n.1928-91A=
ENST00000507018.5:c.1389-91A=
ENST00000509485.5:c.326-91A=
ENST00000514242.5:n.91A=
ENST00000514554.5:c.563-91A=
NM_000358.2:c.1411-91A= NP_000349.1:n.1411-91A=
NM_000358.3:c.1411-91A= MANE Select NP_000349.1:n.1411-91A=
Search 100 bp 5'
Search 100 bp 3'