Linked Data
gnomAD v4:
17-70174971-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70174971C>A , CM000679.2:g.70174971C>A | GRCh38 |
| NC_000017.10:g.68171112C>A , CM000679.1:g.68171112C>A | GRCh37 |
| NC_000017.9:g.65682707C>A | NCBI36 |
| NG_008798.1:g.10437C>A , LRG_328:g.10437C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.-69C>A MANE Select | ENSP00000243457.2:n.-69C>A | |
| ENST00000243457.3:c.-69C>A | ENSP00000243457.2:n.-69C>A | |
| ENST00000535240.1:c.-69C>A | ENSP00000441848.1:n.-69C>A | |
| NM_000891.2:c.-69C>A , LRG_328t1:c.-69C>A | NP_000882.1:n.-69C>A | |
| XM_011524779.1:c.-69C>A | XP_011523081.1:n.-69C>A | |
| NM_000891.3:c.-69C>A MANE Select | NP_000882.1:n.-69C>A |