Linked Data
ClinVar Variation Id:
2189278
ClinVar RCV Id:
RCV002607236
gnomAD v4:
X-47574337-G-A
MyVariant Identifiers:
chrX:g.47433736G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.47574337G>A , CM000685.2:g.47574337G>A | GRCh38 |
| NC_000023.10:g.47433736G>A , CM000685.1:g.47433736G>A | GRCh37 |
| NC_000023.9:g.47318680G>A | NCBI36 |
| NG_008437.1:g.50521C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295987.13:c.1647C>T MANE Select | ENSP00000295987.7:p.Pro549= | |
| ENST00000340666.5:c.1647C>T | ENSP00000343206.4:p.Pro549= | |
| ENST00000640721.1:c.70+351C>T | ENSP00000492857.1:n.70+351C>T | |
| ENST00000295987.11:c.1647C>T | ENSP00000295987.7:p.Pro549= | |
| ENST00000340666.4:c.1647C>T | ENSP00000343206.4:p.Pro549= | |
| NM_006950.3:c.1647C>T MANE Select | NP_008881.2:p.Pro549= | |
| NM_133499.2:c.1647C>T | NP_598006.1:p.Pro549= |