Linked Data
gnomAD v4:
15-97960742-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97960742C>A , CM000677.2:g.97960742C>A | GRCh38 |
| NC_000015.9:g.98503972C>A , CM000677.1:g.98503972C>A | GRCh37 |
| NC_000015.8:g.96304976C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268042.7:c.-120C>A MANE Select | ENSP00000268042.6:n.-120C>A | |
| ENST00000268042.6:c.-120C>A | ENSP00000268042.6:n.-120C>A | |
| NM_183376.2:c.-120C>A | NP_899232.2:n.-120C>A | |
| NM_183376.3:c.-120C>A MANE Select | NP_899232.2:n.-120C>A |