Linked Data
MyVariant Identifiers:
chrX:g.82763268T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508260T>G , CM000685.2:g.83508260T>G | GRCh38 |
| NC_000023.10:g.82763268T>G , CM000685.1:g.82763268T>G | GRCh37 |
| NC_000023.9:g.82649924T>G | NCBI36 |
| NG_009936.2:g.5000T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373200.4:c.-65T>G | ENSP00000362296.2:n.-65T>G |