Canonical Allele Identifier: CA2734901476

Gene: TTR

Linked Data

• dbSNP Id: rs2144409318

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595053T>G , CM000680.2:g.31595053T>G	GRCh38
NC_000018.9:g.29175016T>G , CM000680.1:g.29175016T>G	GRCh37
NC_000018.8:g.27429014T>G	NCBI36
NG_009490.1:g.8287T>G , LRG_416:g.8287T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.201-67T>G MANE Select	ENSP00000237014.4:n.201-67T>G
ENST00000610404.5:c.105-67T>G	ENSP00000477599.2:n.105-67T>G
ENST00000649620.1:c.201-67T>G	ENSP00000497927.1:n.201-67T>G
ENST00000237014.7:c.201-67T>G	ENSP00000237014.3:n.201-67T>G
ENST00000541025.2:n.227-67T>G
ENST00000610404.4:c.201-67T>G	ENSP00000477599.1:n.201-67T>G
ENST00000613781.1:c.201-67T>G	ENSP00000479174.1:n.201-67T>G
NM_000371.3:c.201-67T>G , LRG_416t1:c.201-67T>G	NP_000362.1:n.201-67T>G
NM_000371.4:c.201-67T>G MANE Select	NP_000362.1:n.201-67T>G