Linked Data
dbSNP Id:
rs1557108033
gnomAD v2:
X-49075046-G-A
gnomAD v4:
X-49218587-G-A
MyVariant Identifiers:
chrX:g.49075046G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.49218587G>A , CM000685.2:g.49218587G>A | GRCh38 |
| NC_000023.10:g.49075046G>A , CM000685.1:g.49075046G>A | GRCh37 |
| NC_000023.9:g.48961990G>A | NCBI36 |
| NG_009095.2:g.19780C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323022.10:c.2840+42C>T MANE Select | ENSP00000321618.6:n.2840+42C>T | |
| ENST00000323022.9:c.2840+42C>T | ENSP00000321618.5:n.2840+42C>T | |
| ENST00000376251.5:c.2678+42C>T | ENSP00000365427.1:n.2678+42C>T | |
| ENST00000376265.2:c.2873+42C>T | ENSP00000365441.2:n.2873+42C>T | |
| NM_001256789.2:c.2840+42C>T | NP_001243718.1:n.2840+42C>T | |
| NM_001256790.2:c.2678+42C>T | NP_001243719.1:n.2678+42C>T | |
| NM_005183.3:c.2873+42C>T | NP_005174.2:n.2873+42C>T | |
| XM_011543983.1:c.2678+42C>T | XP_011542285.1:n.2678+42C>T | |
| XM_011543983.2:c.2678+42C>T | XP_011542285.1:n.2678+42C>T | |
| XM_017029836.1:c.107+42C>T | XP_016885325.1:n.107+42C>T | |
| NM_001256789.3:c.2840+42C>T MANE Select | NP_001243718.1:n.2840+42C>T | |
| NM_001256790.3:c.2678+42C>T | NP_001243719.1:n.2678+42C>T | |
| NM_005183.4:c.2873+42C>T | NP_005174.2:n.2873+42C>T |