Linked Data
ClinVar Variation Id:
502493
dbSNP Id:
rs768210143
gnomAD v2:
17-70117547-C-T
gnomAD v3:
17-72121406-C-T
gnomAD v4:
17-72121406-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72121406C>T , CM000679.2:g.72121406C>T | GRCh38 |
| NC_000017.10:g.70117547C>T , CM000679.1:g.70117547C>T | GRCh37 |
| NC_000017.9:g.67629142C>T | NCBI36 |
| NG_012490.1:g.5387C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.15C>T MANE Select | ENSP00000245479.2:p.Asp5= | |
| ENST00000245479.2:c.15C>T | ENSP00000245479.2:p.Asp5= | |
| NM_000346.3:c.15C>T | NP_000337.1:p.Asp5= | |
| NM_000346.4:c.15C>T MANE Select | NP_000337.1:p.Asp5= |