Linked Data
dbSNP Id:
rs761951366
ExAC:
17:39742670 G / A
gnomAD v2:
17-39742670-G-A
gnomAD v4:
17-41586418-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586418G>A , CM000679.2:g.41586418G>A | GRCh38 |
| NC_000017.10:g.39742670G>A , CM000679.1:g.39742670G>A | GRCh37 |
| NC_000017.9:g.36996196G>A | NCBI36 |
| NG_008624.1:g.5478C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.417C>T MANE Select | ENSP00000167586.6:p.Ala139= | |
| ENST00000167586.6:c.417C>T | ENSP00000167586.6:p.Ala139= | |
| NM_000526.4:c.417C>T | NP_000517.2:p.Ala139= | |
| NM_000526.5:c.417C>T MANE Select | NP_000517.3:p.Ala139= |