Linked Data
dbSNP Id:
rs1478574927
gnomAD v3:
X-154097859-G-A
gnomAD v4:
X-154097859-G-A
MyVariant Identifiers:
chrX:g.154097859G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097859G>A , CM000685.2:g.154097859G>A | GRCh38 |
| NC_000023.10:g.153363316G>A , CM000685.1:g.153363316G>A | GRCh37 |
| NC_000023.9:g.153016510G>A | NCBI36 |
| NG_007107.2:g.44263C>T | |
| NG_007107.3:g.44245C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6922C>T |