Linked Data
dbSNP Id:
rs1292815132
gnomAD v3:
X-101348831-C-T
gnomAD v4:
X-101348831-C-T
MyVariant Identifiers:
chrX:g.101348831C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348831C>T , CM000685.2:g.101348831C>T | GRCh38 |
| NC_000023.10:g.100603819C>T , CM000685.1:g.100603819C>T | GRCh37 |
| NC_000023.9:g.100490475C>T | NCBI36 |
| NG_009616.1:g.42394G>A , LRG_128:g.42394G>A | |
| NG_011734.1:g.5139G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.3:c.-167G>A | ENSP00000361993.3:n.-167G>A | |
| NM_004085.3:c.-167G>A | NP_004076.1:n.-167G>A |