Linked Data
ClinVar Variation Id:
1125296
ClinVar RCV Id:
RCV001456993
dbSNP Id:
rs1458553359
gnomAD v2:
X-53432476-G-A
gnomAD v4:
X-53405544-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.53405544G>A , CM000685.2:g.53405544G>A | GRCh38 |
| NC_000023.10:g.53432476G>A , CM000685.1:g.53432476G>A | GRCh37 |
| NC_000023.9:g.53449201G>A | NCBI36 |
| NG_006988.2:g.22127C>T , LRG_773:g.22127C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322213.9:c.1860C>T MANE Select | ENSP00000323421.3:p.Asp620= | |
| ENST00000674590.1:c.1092C>T | ENSP00000502626.1:p.Asp364= | |
| ENST00000675065.1:n.1212C>T | ||
| ENST00000675504.1:c.1794C>T | ENSP00000502524.1:p.Asp598= | |
| ENST00000322213.8:c.1860C>T | ENSP00000323421.3:p.Asp620= | |
| ENST00000375340.10:c.1794C>T | ENSP00000364489.7:p.Asp598= | |
| NM_001281463.1:c.1794C>T , LRG_773t1:c.1794C>T | NP_001268392.1:p.Asp598= | |
| NM_006306.3:c.1860C>T , LRG_773t2:c.1860C>T | NP_006297.2:p.Asp620= | |
| NM_006306.4:c.1860C>T MANE Select | NP_006297.2:p.Asp620= |