Linked Data
dbSNP Id:
rs1488734636
gnomAD v3:
X-83508251-C-CCCGCA
gnomAD v4:
X-83508251-C-CCCGCA
MyVariant Identifiers:
chrX:g.82763259_82763260insCCGCA (hg19)
chrX:g.83508251_83508252insCCGCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508255_83508259dup , CM000685.2:g.83508255_83508259dup | GRCh38 |
| NC_000023.10:g.82763263_82763267dup , CM000685.1:g.82763263_82763267dup | GRCh37 |
| NC_000023.9:g.82649919_82649923dup | NCBI36 |
| NG_009936.2:g.4995_4999dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373200.4:c.-70_-66dup | ENSP00000362296.2:n.-70_-66dup |