Canonical Allele Identifier: CA361041841
Gene: TGFBI HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135392434C>A (hg19) chr5:g.136056745C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056745C>A , CM000667.2:g.136056745C>A GRCh38
NC_000005.9:g.135392434C>A , CM000667.1:g.135392434C>A GRCh37
NC_000005.8:g.135420333C>A NCBI36
NG_012646.1:g.32851C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1628C>A MANE Select ENSP00000416330.2:p.Thr543Lys
ENST00000442011.6:c.1628C>A ENSP00000416330.2:p.Thr543Lys
ENST00000506699.5:n.2145C>A
ENST00000507018.5:c.1606C>A
ENST00000509485.5:c.625C>A
ENST00000514242.5:n.399C>A
ENST00000514554.5:c.780C>A
NM_000358.2:c.1628C>A NP_000349.1:p.Thr543Lys
NM_000358.3:c.1628C>A MANE Select NP_000349.1:p.Thr543Lys
Search 100 bp 5'
Search 100 bp 3'