Linked Data
dbSNP Id:
rs1160807462
gnomAD v3:
X-101348746-T-C
gnomAD v4:
X-101348746-T-C
MyVariant Identifiers:
chrX:g.101348746T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348746T>C , CM000685.2:g.101348746T>C | GRCh38 |
| NC_000023.10:g.100603734T>C , CM000685.1:g.100603734T>C | GRCh37 |
| NC_000023.9:g.100490390T>C | NCBI36 |
| NG_009616.1:g.42479A>G , LRG_128:g.42479A>G | |
| NG_011734.1:g.5224A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.3:c.-82A>G | ENSP00000361993.3:n.-82A>G | |
| ENST00000480575.1:n.4A>G | ||
| NM_004085.3:c.-82A>G | NP_004076.1:n.-82A>G |