Canonical Allele Identifier: CA297741794
Gene: TTR HGNC NCBI

Linked Data

dbSNP Id: rs908086070
gnomAD v2: 18-29178512-T-C
MyVariant Identifiers: chr18:g.29178512T>C (hg19) chr18:g.31598549T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598549T>C , CM000680.2:g.31598549T>C GRCh38
NC_000018.9:g.29178512T>C , CM000680.1:g.29178512T>C GRCh37
NC_000018.8:g.27432510T>C NCBI36
NG_009490.1:g.11783T>C , LRG_416:g.11783T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-19T>C MANE Select ENSP00000237014.4:n.337-19T>C
ENST00000610404.5:c.241-19T>C ENSP00000477599.2:n.241-19T>C
ENST00000649620.1:c.337-19T>C ENSP00000497927.1:n.337-19T>C
ENST00000237014.7:c.337-19T>C ENSP00000237014.3:n.337-19T>C
ENST00000610404.4:c.451-19T>C ENSP00000477599.1:n.451-19T>C
ENST00000613781.1:c.337-19T>C ENSP00000479174.1:n.337-19T>C
NM_000371.3:c.337-19T>C , LRG_416t1:c.337-19T>C NP_000362.1:n.337-19T>C
NM_000371.4:c.337-19T>C MANE Select NP_000362.1:n.337-19T>C
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