Canonical Allele Identifier: CA503610159
Gene: TTR HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29172960T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592997T>A , CM000680.2:g.31592997T>A GRCh38
NC_000018.9:g.29172960T>A , CM000680.1:g.29172960T>A GRCh37
NC_000018.8:g.27426958T>A NCBI36
NG_009490.1:g.6231T>A , LRG_416:g.6231T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.171T>A MANE Select ENSP00000237014.4:p.Ala57=
ENST00000610404.5:c.75T>A ENSP00000477599.2:p.Ala25=
ENST00000649620.1:c.171T>A ENSP00000497927.1:p.Ala57=
ENST00000237014.7:c.171T>A ENSP00000237014.3:p.Ala57=
ENST00000432547.7:n.197T>A
ENST00000541025.2:n.197T>A
ENST00000610404.4:c.171T>A ENSP00000477599.1:p.Ala57=
ENST00000613781.1:c.171T>A ENSP00000479174.1:p.Ala57=
NM_000371.3:c.171T>A , LRG_416t1:c.171T>A NP_000362.1:p.Ala57=
NM_000371.4:c.171T>A MANE Select NP_000362.1:p.Ala57=
Search 100 bp 5'
Search 100 bp 3'