Linked Data
gnomAD v4:
9-69035714-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.69035714C>A , CM000671.2:g.69035714C>A | GRCh38 |
| NC_000009.11:g.71650630C>A , CM000671.1:g.71650630C>A | GRCh37 |
| NC_000009.10:g.70840450C>A | NCBI36 |
| NG_008845.2:g.5152C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377270.7:c.-69C>A | ENSP00000366482.3:n.-69C>A | |
| ENST00000396364.7:c.-69C>A | ENSP00000379650.3:n.-69C>A | |
| NM_000144.4:c.-69C>A | NP_000135.2:n.-69C>A | |
| NM_001161706.1:c.-69C>A | NP_001155178.1:n.-69C>A | |
| NM_181425.2:c.-69C>A | NP_852090.1:n.-69C>A |