Linked Data
gnomAD v4:
X-154097895-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097895C>A , CM000685.2:g.154097895C>A | GRCh38 |
| NC_000023.10:g.153363353C>A , CM000685.1:g.153363353C>A | GRCh37 |
| NC_000023.9:g.153016547C>A | NCBI36 |
| NG_007107.2:g.44226G>T | |
| NG_007107.3:g.44209G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6886G>T |