Linked Data
ClinVar Variation Id:
1085983
dbSNP Id:
rs2146581314
MyVariant Identifiers:
chrX:g.53407604G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53380683G>A , CM000685.2:g.53380683G>A | GRCh38 |
| NC_000023.10:g.53407604G>A , CM000685.1:g.53407604G>A | GRCh37 |
| NC_000023.9:g.53424329G>A | NCBI36 |
| NG_006988.2:g.46988C>T , LRG_773:g.46988C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322213.9:c.3555C>T MANE Select | ENSP00000323421.3:p.Ile1185= | |
| ENST00000674590.1:c.2787C>T | ENSP00000502626.1:p.Ile929= | |
| ENST00000675504.1:c.3489C>T | ENSP00000502524.1:p.Ile1163= | |
| ENST00000322213.8:c.3555C>T | ENSP00000323421.3:p.Ile1185= | |
| ENST00000375340.10:c.3489C>T | ENSP00000364489.7:p.Ile1163= | |
| ENST00000470241.2:c.775C>T | ||
| NM_001281463.1:c.3489C>T , LRG_773t1:c.3489C>T | NP_001268392.1:p.Ile1163= | |
| NM_006306.3:c.3555C>T , LRG_773t2:c.3555C>T | NP_006297.2:p.Ile1185= | |
| NM_006306.4:c.3555C>T MANE Select | NP_006297.2:p.Ile1185= |