Canonical Allele Identifier: CA503610836
Gene: TTR HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29178542A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598579A>C , CM000680.2:g.31598579A>C GRCh38
NC_000018.9:g.29178542A>C , CM000680.1:g.29178542A>C GRCh37
NC_000018.8:g.27432540A>C NCBI36
NG_009490.1:g.11813A>C , LRG_416:g.11813A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.348A>C MANE Select ENSP00000237014.4:p.Thr116=
ENST00000610404.5:c.252A>C ENSP00000477599.2:p.Thr84=
ENST00000649620.1:c.348A>C ENSP00000497927.1:p.Thr116=
ENST00000237014.7:c.348A>C ENSP00000237014.3:p.Thr116=
ENST00000610404.4:c.462A>C ENSP00000477599.1:p.Thr154=
ENST00000613781.1:c.348A>C ENSP00000479174.1:p.Thr116=
NM_000371.3:c.348A>C , LRG_416t1:c.348A>C NP_000362.1:p.Thr116=
NM_000371.4:c.348A>C MANE Select NP_000362.1:p.Thr116=
Search 100 bp 5'
Search 100 bp 3'