Canonical Allele Identifier: CA503609790
Gene: TTR HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29172861C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592898C>A , CM000680.2:g.31592898C>A GRCh38
NC_000018.9:g.29172861C>A , CM000680.1:g.29172861C>A GRCh37
NC_000018.8:g.27426859C>A NCBI36
NG_009490.1:g.6132C>A , LRG_416:g.6132C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.72C>A MANE Select ENSP00000237014.4:p.Gly24=
ENST00000610404.5:c.-25C>A ENSP00000477599.2:n.-25C>A
ENST00000649620.1:c.72C>A ENSP00000497927.1:p.Gly24=
ENST00000237014.7:c.72C>A ENSP00000237014.3:p.Gly24=
ENST00000432547.7:n.98C>A
ENST00000541025.2:n.98C>A
ENST00000610404.4:c.72C>A ENSP00000477599.1:p.Gly24=
ENST00000613781.1:c.72C>A ENSP00000479174.1:p.Gly24=
NM_000371.3:c.72C>A , LRG_416t1:c.72C>A NP_000362.1:p.Gly24=
NM_000371.4:c.72C>A MANE Select NP_000362.1:p.Gly24=