Linked Data
ClinVar Variation Id:
98699
dbSNP Id:
rs61755810
ExAC:
6:42672272 C / T
gnomAD v2:
6-42672272-C-T
gnomAD v3:
6-42704534-C-T
gnomAD v4:
6-42704534-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42704534C>T , CM000668.2:g.42704534C>T | GRCh38 |
| NC_000006.11:g.42672272C>T , CM000668.1:g.42672272C>T | GRCh37 |
| NC_000006.10:g.42780250C>T | NCBI36 |
| NG_009176.1:g.23087G>A | |
| NG_009176.2:g.23087G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.659G>A MANE Select | ENSP00000230381.5:p.Arg220Gln | |
| ENST00000230381.6:c.659G>A | ENSP00000230381.5:p.Arg220Gln | |
| NM_000322.4:c.659G>A | NP_000313.2:p.Arg220Gln | |
| XR_427834.2:n.1314G>A | ||
| XR_926295.1:n.1496G>A | ||
| XR_427834.4:n.1364G>A | ||
| XR_926295.3:n.1546G>A | ||
| NM_000322.5:c.659G>A MANE Select | NP_000313.2:p.Arg220Gln |