Linked Data
dbSNP Id:
rs1569559789
gnomAD v4:
X-154953902-G-A
MyVariant Identifiers:
chrX:g.154182177G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154953902G>A , CM000685.2:g.154953902G>A | GRCh38 |
| NC_000023.10:g.154182177G>A , CM000685.1:g.154182177G>A | GRCh37 |
| NC_000023.9:g.153835371G>A | NCBI36 |
| NG_011403.1:g.73822C>T | |
| NG_011403.2:g.73822C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1893C>T MANE Select | ENSP00000353393.4:p.Asn631= | |
| ENST00000647125.1:c.*1769C>T | ENSP00000496062.1:n.*1769C>T | |
| ENST00000360256.8:c.1893C>T | ENSP00000353393.4:p.Asn631= | |
| NM_000132.3:c.1893C>T | NP_000123.1:p.Asn631= | |
| XM_011531126.1:c.1788C>T | XP_011529428.1:p.Asn596= | |
| NM_000132.4:c.1893C>T MANE Select | NP_000123.1:p.Asn631= |