Linked Data
gnomAD v4:
X-154097900-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097900C>T , CM000685.2:g.154097900C>T | GRCh38 |
| NC_000023.10:g.153363358C>T , CM000685.1:g.153363358C>T | GRCh37 |
| NC_000023.9:g.153016552C>T | NCBI36 |
| NG_007107.2:g.44221G>A | |
| NG_007107.3:g.44204G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6881G>A |