Linked Data
dbSNP Id:
rs1455782617
gnomAD v3:
X-154379219-GCCTC-G
gnomAD v4:
X-154379219-GCCTC-G
MyVariant Identifiers:
chrX:g.154379220_154379223del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379222_154379225del , CM000685.2:g.154379222_154379225del | GRCh38 |
| NC_000023.10:g.153607582_153607585del , CM000685.1:g.153607582_153607585del | GRCh37 |
| NC_000023.9:g.153260776_153260779del | NCBI36 |
| NG_008677.1:g.9787_9790del , LRG_745:g.9787_9790del | |
| NG_011506.1:g.424_427del | |
| NG_011506.2:g.416_419del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.8:c.-263_-260del | ENSP00000358857.4:n.-263_-260del |