Linked Data
gnomAD v4:
15-97960835-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97960835A>C , CM000677.2:g.97960835A>C | GRCh38 |
| NC_000015.9:g.98504065A>C , CM000677.1:g.98504065A>C | GRCh37 |
| NC_000015.8:g.96305069A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268042.7:c.-27A>C MANE Select | ENSP00000268042.6:n.-27A>C | |
| ENST00000268042.6:c.-27A>C | ENSP00000268042.6:n.-27A>C | |
| NM_183376.2:c.-27A>C | NP_899232.2:n.-27A>C | |
| NM_183376.3:c.-27A>C MANE Select | NP_899232.2:n.-27A>C |