Canonical Allele Identifier: CA2293886764
Gene: TTR HGNC NCBI

Linked Data

dbSNP Id: rs1567945584
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592849A>T , CM000680.2:g.31592849A>T GRCh38
NC_000018.9:g.29172812A>T , CM000680.1:g.29172812A>T GRCh37
NC_000018.8:g.27426810A>T NCBI36
NG_009490.1:g.6083A>T , LRG_416:g.6083A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.70-47A>T MANE Select ENSP00000237014.4:n.70-47A>T
ENST00000610404.5:c.-27-47A>T ENSP00000477599.2:n.-27-47A>T
ENST00000649620.1:c.70-47A>T ENSP00000497927.1:n.70-47A>T
ENST00000237014.7:c.70-47A>T ENSP00000237014.3:n.70-47A>T
ENST00000432547.7:n.96-47A>T
ENST00000541025.2:n.96-47A>T
ENST00000610404.4:c.70-47A>T ENSP00000477599.1:n.70-47A>T
ENST00000613781.1:c.70-47A>T ENSP00000479174.1:n.70-47A>T
NM_000371.3:c.70-47A>T , LRG_416t1:c.70-47A>T NP_000362.1:n.70-47A>T
NM_000371.4:c.70-47A>T MANE Select NP_000362.1:n.70-47A>T
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