Canonical Allele Identifier: CA123106
Gene: TTR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13452
dbSNP Id: rs1800458

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592902G>A , CM000680.2:g.31592902G>A GRCh38
NC_000018.9:g.29172865G>A , CM000680.1:g.29172865G>A GRCh37
NC_000018.8:g.27426863G>A NCBI36
NG_009490.1:g.6136G>A , LRG_416:g.6136G>A

Transcript Alleles

HGVS Amino-acid change
NM_000371.3:c.76G>A , LRG_416t1:c.76G>A NP_000362.1:p.Gly26Ser
ENST00000237014.7:c.76G>A ENSP00000237014.3:p.Gly26Ser
ENST00000432547.7:n.102G>A
ENST00000541025.2:n.102G>A
ENST00000610404.4:c.76G>A ENSP00000477599.1:p.Gly26Ser
ENST00000613781.1:c.76G>A ENSP00000479174.1:p.Gly26Ser