Linked Data
ClinVar Variation Id:
1914328
ClinVar RCV Id:
RCV002597463
dbSNP Id:
rs755349243
gnomAD v2:
1-1471149-C-T
gnomAD v3:
1-1535769-C-T
gnomAD v4:
1-1535769-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1535769C>T , CM000663.2:g.1535769C>T | GRCh38 |
| NC_000001.10:g.1471149C>T , CM000663.1:g.1471149C>T | GRCh37 |
| NC_000001.9:g.1461012C>T | NCBI36 |
| NG_041807.1:g.9592G>A | |
| NG_053035.1:g.28627C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378733.9:c.193G>A MANE Select | ENSP00000368007.4:p.Asp65Asn | |
| ENST00000378733.8:c.193G>A | ENSP00000368007.4:p.Asp65Asn | |
| ENST00000425828.1:c.193G>A | ENSP00000400311.1:p.Asp65Asn | |
| NM_001114748.1:c.193G>A | NP_001108220.1:p.Asp65Asn | |
| NM_001114748.2:c.193G>A MANE Select | NP_001108220.1:p.Asp65Asn |