Linked Data
ClinVar Variation Id:
2158528
dbSNP Id:
rs762787977
ExAC:
1:1471077 C / T
gnomAD v2:
1-1471077-C-T
gnomAD v3:
1-1535697-C-T
gnomAD v4:
1-1535697-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1535697C>T , CM000663.2:g.1535697C>T | GRCh38 |
| NC_000001.10:g.1471077C>T , CM000663.1:g.1471077C>T | GRCh37 |
| NC_000001.9:g.1460940C>T | NCBI36 |
| NG_041807.1:g.9664G>A | |
| NG_053035.1:g.28555C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378733.9:c.265G>A MANE Select | ENSP00000368007.4:p.Asp89Asn | |
| ENST00000378733.8:c.265G>A | ENSP00000368007.4:p.Asp89Asn | |
| ENST00000425828.1:c.265G>A | ENSP00000400311.1:p.Asp89Asn | |
| NM_001114748.1:c.265G>A | NP_001108220.1:p.Asp89Asn | |
| NM_001114748.2:c.265G>A MANE Select | NP_001108220.1:p.Asp89Asn |