Linked Data
MyVariant Identifiers:
chrX:g.82763285A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508277A>C , CM000685.2:g.83508277A>C | GRCh38 |
| NC_000023.10:g.82763285A>C , CM000685.1:g.82763285A>C | GRCh37 |
| NC_000023.9:g.82649941A>C | NCBI36 |
| NG_009936.2:g.5017A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373200.4:c.-48A>C | ENSP00000362296.2:n.-48A>C | |
| NM_000307.4:c.-48A>C | NP_000298.3:n.-48A>C |