Linked Data
dbSNP Id:
rs1259722284
gnomAD v3:
X-101348792-G-A
gnomAD v4:
X-101348792-G-A
MyVariant Identifiers:
chrX:g.101348792G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348792G>A , CM000685.2:g.101348792G>A | GRCh38 |
| NC_000023.10:g.100603780G>A , CM000685.1:g.100603780G>A | GRCh37 |
| NC_000023.9:g.100490436G>A | NCBI36 |
| NG_009616.1:g.42433C>T , LRG_128:g.42433C>T | |
| NG_011734.1:g.5178C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.3:c.-128C>T | ENSP00000361993.3:n.-128C>T | |
| NM_004085.3:c.-128C>T | NP_004076.1:n.-128C>T |