Linked Data
dbSNP Id:
rs1207079690
gnomAD v3:
X-116173462-A-G
gnomAD v4:
X-116173462-A-G
MyVariant Identifiers:
chrX:g.116173462A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116173462A>G , CM000685.2:g.116173462A>G | GRCh38 |
| NC_000023.10:g.115304715A>G , CM000685.1:g.115304715A>G | GRCh37 |
| NC_000023.9:g.115218743A>G | NCBI36 |
| NG_016326.1:g.7758A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.*90A>G MANE Select | ENSP00000360973.4:n.*90A>G | |
| ENST00000371906.4:c.*90A>G | ENSP00000360973.4:n.*90A>G | |
| NM_000686.4:c.*90A>G | NP_000677.2:n.*90A>G | |
| XM_011537533.1:c.*90A>G | XP_011535835.1:n.*90A>G | |
| NM_000686.5:c.*90A>G MANE Select | NP_000677.2:n.*90A>G | |
| NM_001385624.1:c.*90A>G | NP_001372553.1:n.*90A>G |