Linked Data
ClinVar Variation Id:
2937974
ClinVar RCV Id:
RCV003796796
gnomAD v4:
X-18628559-G-A
MyVariant Identifiers:
chrX:g.18646679G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18628559G>A , CM000685.2:g.18628559G>A | GRCh38 |
| NC_000023.10:g.18646679G>A , CM000685.1:g.18646679G>A | GRCh37 |
| NC_000023.9:g.18556600G>A | NCBI36 |
| NG_008475.1:g.207955G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623535.2:c.2685G>A MANE Select | ENSP00000485244.1:p.Pro895= | |
| ENST00000674046.1:c.2808G>A | ENSP00000501174.1:p.Pro936= | |
| ENST00000379989.6:c.2685G>A | ENSP00000369325.3:p.Pro895= | |
| ENST00000379996.7:c.2685G>A | ENSP00000369332.3:p.Pro895= | |
| ENST00000623535.1:c.2685G>A | ENSP00000485244.1:p.Pro895= | |
| NM_001037343.1:c.2685G>A | NP_001032420.1:p.Pro895= | |
| NM_003159.2:c.2685G>A | NP_003150.1:p.Pro895= | |
| XM_011545569.1:c.2757G>A | XP_011543871.1:p.Pro919= | |
| XM_011545570.1:c.2676G>A | XP_011543872.1:p.Pro892= | |
| XR_950484.1:n.3060G>A | ||
| NM_001323289.1:c.2685G>A | NP_001310218.1:p.Pro895= | |
| NM_001323289.2:c.2685G>A MANE Select | NP_001310218.1:p.Pro895= | |
| NM_001037343.2:c.2685G>A | NP_001032420.1:p.Pro895= | |
| NM_003159.3:c.2685G>A | NP_003150.1:p.Pro895= |