Linked Data
gnomAD v4:
X-154097890-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097890A>T , CM000685.2:g.154097890A>T | GRCh38 |
| NC_000023.10:g.153363348A>T , CM000685.1:g.153363348A>T | GRCh37 |
| NC_000023.9:g.153016542A>T | NCBI36 |
| NG_007107.2:g.44231T>A | |
| NG_007107.3:g.44214T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6891T>A |