Canonical Allele Identifier: CA2293886591

Gene: TTR

Linked Data

• dbSNP Id: rs2073490659

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592417T>C , CM000680.2:g.31592417T>C	GRCh38
NC_000018.9:g.29172380T>C , CM000680.1:g.29172380T>C	GRCh37
NC_000018.8:g.27426378T>C	NCBI36
NG_009490.1:g.5651T>C , LRG_416:g.5651T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.69+446T>C MANE Select	ENSP00000237014.4:n.69+446T>C
ENST00000610404.5:c.-27-479T>C	ENSP00000477599.2:n.-27-479T>C
ENST00000649620.1:c.69+446T>C	ENSP00000497927.1:n.69+446T>C
ENST00000237014.7:c.69+446T>C	ENSP00000237014.3:n.69+446T>C
ENST00000432547.7:n.95+446T>C
ENST00000541025.2:n.95+446T>C
ENST00000610404.4:c.69+446T>C	ENSP00000477599.1:n.69+446T>C
ENST00000613781.1:c.69+446T>C	ENSP00000479174.1:n.69+446T>C
NM_000371.3:c.69+446T>C , LRG_416t1:c.69+446T>C	NP_000362.1:n.69+446T>C
NM_000371.4:c.69+446T>C MANE Select	NP_000362.1:n.69+446T>C