Linked Data
dbSNP Id:
rs1020056918
gnomAD v3:
X-46836986-G-T
gnomAD v4:
X-46836986-G-T
MyVariant Identifiers:
chrX:g.46836986G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46836986G>T , CM000685.2:g.46836986G>T | GRCh38 |
| NC_000023.10:g.46696421G>T , CM000685.1:g.46696421G>T | GRCh37 |
| NC_000023.9:g.46581365G>T | NCBI36 |
| NG_009107.1:g.5075G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218340.3:c.-115G>T | ENSP00000218340.3:n.-115G>T | |
| NM_006915.2:c.-115G>T | NP_008846.2:n.-115G>T |