Linked Data
dbSNP Id:
rs1444776004
gnomAD v3:
X-154097865-G-C
gnomAD v4:
X-154097865-G-C
MyVariant Identifiers:
chrX:g.154097865G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097865G>C , CM000685.2:g.154097865G>C | GRCh38 |
| NC_000023.10:g.153363322G>C , CM000685.1:g.153363322G>C | GRCh37 |
| NC_000023.9:g.153016516G>C | NCBI36 |
| NG_007107.2:g.44257C>G | |
| NG_007107.3:g.44239C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6916C>G |