Linked Data
gnomAD v4:
X-154097762-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097762C>G , CM000685.2:g.154097762C>G | GRCh38 |
| NC_000023.10:g.153363219C>G , CM000685.1:g.153363219C>G | GRCh37 |
| NC_000023.9:g.153016413C>G | NCBI36 |
| NG_007107.2:g.44360G>C | |
| NG_007107.3:g.44342G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453960.6:c.-97G>C | ENSP00000395535.2:n.-97G>C | |
| ENST00000631210.1:n.305+7019G>C |