Linked Data
dbSNP Id:
rs1358149873
gnomAD v3:
X-154379257-T-C
gnomAD v4:
X-154379257-T-C
MyVariant Identifiers:
chrX:g.154379257T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379257T>C , CM000685.2:g.154379257T>C | GRCh38 |
| NC_000023.10:g.153607617T>C , CM000685.1:g.153607617T>C | GRCh37 |
| NC_000023.9:g.153260811T>C | NCBI36 |
| NG_008677.1:g.9822T>C , LRG_745:g.9822T>C | |
| NG_011506.1:g.390A>G | |
| NG_011506.2:g.382A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.8:c.-228T>C | ENSP00000358857.4:n.-228T>C | |
| NM_000117.2:c.-228T>C , LRG_745t1:c.-228T>C | NP_000108.1:n.-228T>C | |
| XM_024452349.1:c.-436T>C | XP_024308117.1:n.-436T>C |