Linked Data
dbSNP Id:
rs1557285136
gnomAD v2:
X-154225245-C-T
gnomAD v4:
X-154996970-C-T
MyVariant Identifiers:
chrX:g.154225245C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154996970C>T , CM000685.2:g.154996970C>T | GRCh38 |
| NC_000023.10:g.154225245C>T , CM000685.1:g.154225245C>T | GRCh37 |
| NC_000023.9:g.153878439C>T | NCBI36 |
| NG_011403.1:g.30754G>A | |
| NG_011403.2:g.30754G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.388+3G>A MANE Select | ENSP00000353393.4:n.388+3G>A | |
| ENST00000647125.1:c.*174+3G>A | ENSP00000496062.1:n.*174+3G>A | |
| ENST00000360256.8:c.388+3G>A | ENSP00000353393.4:n.388+3G>A | |
| ENST00000423959.5:c.283+3G>A | ENSP00000409446.1:n.283+3G>A | |
| ENST00000453950.1:c.370+3G>A | ENSP00000389153.1:n.370+3G>A | |
| NM_000132.3:c.388+3G>A | NP_000123.1:n.388+3G>A | |
| XM_011531126.1:c.283+3G>A | XP_011529428.1:n.283+3G>A | |
| NM_000132.4:c.388+3G>A MANE Select | NP_000123.1:n.388+3G>A |