Linked Data
dbSNP Id:
rs1208543899
gnomAD v3:
X-154191619-C-G
gnomAD v4:
X-154191619-C-G
MyVariant Identifiers:
chrX:g.154191619C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154191619C>G , CM000685.2:g.154191619C>G | GRCh38 |
| NC_000023.10:g.153457110C>G , CM000685.1:g.153457110C>G | GRCh37 |
| NG_011606.1:g.14026C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000595290.6:c.579-69C>G MANE Select | ENSP00000472316.1:n.579-69C>G | |
| ENST00000595290.5:c.579-69C>G | ENSP00000472316.1:n.579-69C>G | |
| ENST00000595330.1:n.588+1397C>G | ||
| ENST00000596998.2:c.166-69C>G | ||
| NM_000513.2:c.579-69C>G MANE Select | NP_000504.1:n.579-69C>G |