Linked Data
gnomAD v4:
X-154097902-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097902G>T , CM000685.2:g.154097902G>T | GRCh38 |
| NC_000023.10:g.153363360G>T , CM000685.1:g.153363360G>T | GRCh37 |
| NC_000023.9:g.153016554G>T | NCBI36 |
| NG_007107.2:g.44219C>A | |
| NG_007107.3:g.44202C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6879C>A |