Canonical Allele Identifier: CA402156921
Gene: TTR HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29175099G>C (hg19) chr18:g.31595136G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31595136G>C , CM000680.2:g.31595136G>C GRCh38
NC_000018.9:g.29175099G>C , CM000680.1:g.29175099G>C GRCh37
NC_000018.8:g.27429097G>C NCBI36
NG_009490.1:g.8370G>C , LRG_416:g.8370G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.217G>C MANE Select ENSP00000237014.4:p.Gly73Arg
ENST00000610404.5:c.121G>C ENSP00000477599.2:p.Gly41Arg
ENST00000649620.1:c.217G>C ENSP00000497927.1:p.Gly73Arg
ENST00000237014.7:c.217G>C ENSP00000237014.3:p.Gly73Arg
ENST00000541025.2:n.243G>C
ENST00000610404.4:c.217G>C ENSP00000477599.1:p.Gly73Arg
ENST00000613781.1:c.217G>C ENSP00000479174.1:p.Gly73Arg
NM_000371.3:c.217G>C , LRG_416t1:c.217G>C NP_000362.1:p.Gly73Arg
NM_000371.4:c.217G>C MANE Select NP_000362.1:p.Gly73Arg
Search 100 bp 5'
Search 100 bp 3'