Linked Data
gnomAD v4:
17-41586420-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586420C>A , CM000679.2:g.41586420C>A | GRCh38 |
| NC_000017.10:g.39742672C>A , CM000679.1:g.39742672C>A | GRCh37 |
| NC_000017.9:g.36996198C>A | NCBI36 |
| NG_008624.1:g.5476G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.415G>T MANE Select | ENSP00000167586.6:p.Ala139Ser | |
| ENST00000167586.6:c.415G>T | ENSP00000167586.6:p.Ala139Ser | |
| NM_000526.4:c.415G>T | NP_000517.2:p.Ala139Ser | |
| NM_000526.5:c.415G>T MANE Select | NP_000517.3:p.Ala139Ser |