Linked Data
ClinVar Variation Id:
1570712
ClinVar RCV Id:
RCV002215580
dbSNP Id:
rs2147667643
gnomAD v4:
X-85958972-C-T
MyVariant Identifiers:
chrX:g.85213977C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.85958972C>T , CM000685.2:g.85958972C>T | GRCh38 |
| NC_000023.10:g.85213977C>T , CM000685.1:g.85213977C>T | GRCh37 |
| NC_000023.9:g.85100633C>T | NCBI36 |
| NG_009874.2:g.93591G>A , LRG_699:g.93591G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357749.7:c.708G>A MANE Select | ENSP00000350386.2:p.Leu236= | |
| ENST00000357749.6:c.708G>A | ENSP00000350386.2:p.Leu236= | |
| ENST00000467744.2:n.126+68519G>A | ||
| NM_000390.2:c.708G>A , LRG_699t1:c.708G>A | NP_000381.1:p.Leu236= | |
| XM_006724615.2:c.645G>A | XP_006724678.1:p.Leu215= | |
| XM_011530839.1:c.264G>A | XP_011529141.1:p.Leu88= | |
| NM_000390.3:c.708G>A | NP_000381.1:p.Leu236= | |
| NM_001320959.1:c.264G>A | NP_001307888.1:p.Leu88= | |
| NM_001362517.1:c.264G>A | NP_001349446.1:p.Leu88= | |
| NM_001362518.1:c.264G>A | NP_001349447.1:p.Leu88= | |
| NM_001362519.1:c.264G>A | NP_001349448.1:p.Leu88= | |
| XM_017029242.2:c.708G>A | XP_016884731.1:p.Leu236= | |
| XM_017029246.1:c.264G>A | XP_016884735.1:p.Leu88= | |
| XM_024452331.1:c.264G>A | XP_024308099.1:p.Leu88= | |
| NM_000390.4:c.708G>A MANE Select | NP_000381.1:p.Leu236= | |
| NM_001362518.2:c.264G>A | NP_001349447.1:p.Leu88= |