Canonical Allele Identifier: CA503610049

Gene: TTR

Linked Data

• ClinVar Variation Id: 538167
• ClinVar RCV Id: RCV000647359 ; RCV002388114 ; RCV002499104
• dbSNP Id: rs1252826226
• gnomAD v4: 18-31592967-T-C
• MyVariant Identifiers: chr18:g.29172930T>C (hg19) ; chr18:g.31592967T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592967T>C , CM000680.2:g.31592967T>C	GRCh38
NC_000018.9:g.29172930T>C , CM000680.1:g.29172930T>C	GRCh37
NC_000018.8:g.27426928T>C	NCBI36
NG_009490.1:g.6201T>C , LRG_416:g.6201T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.141T>C MANE Select	ENSP00000237014.4:p.Asn47=
ENST00000610404.5:c.45T>C	ENSP00000477599.2:p.Asn15=
ENST00000649620.1:c.141T>C	ENSP00000497927.1:p.Asn47=
ENST00000237014.7:c.141T>C	ENSP00000237014.3:p.Asn47=
ENST00000432547.7:n.167T>C
ENST00000541025.2:n.167T>C
ENST00000610404.4:c.141T>C	ENSP00000477599.1:p.Asn47=
ENST00000613781.1:c.141T>C	ENSP00000479174.1:p.Asn47=
NM_000371.3:c.141T>C , LRG_416t1:c.141T>C	NP_000362.1:p.Asn47=
NM_000371.4:c.141T>C MANE Select	NP_000362.1:p.Asn47=