Linked Data
ClinVar Variation Id:
2837023
ClinVar RCV Id:
RCV003692359
dbSNP Id:
rs1567023092
MyVariant Identifiers:
chr15:g.28096562G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.27851416G>T , CM000677.2:g.27851416G>T | GRCh38 |
| NC_000015.9:g.28096562G>T , CM000677.1:g.28096562G>T | GRCh37 |
| NC_000015.8:g.25770157G>T | NCBI36 |
| NG_009846.1:g.252897C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354638.8:c.2304C>A MANE Select | ENSP00000346659.3:p.Leu768= | |
| ENST00000353809.9:c.2232C>A | ENSP00000261276.8:p.Leu744= | |
| ENST00000354638.7:c.2304C>A | ENSP00000346659.3:p.Leu768= | |
| NM_000275.2:c.2304C>A | NP_000266.2:p.Leu768= | |
| NM_001300984.1:c.2232C>A | NP_001287913.1:p.Leu744= | |
| XM_011521639.1:c.2370C>A | XP_011519941.1:p.Leu790= | |
| XM_011521640.1:c.2346C>A | XP_011519942.1:p.Leu782= | |
| XM_011521641.1:c.2328C>A | XP_011519943.1:p.Leu776= | |
| XM_011521642.1:c.2298C>A | XP_011519944.1:p.Leu766= | |
| XM_011521643.1:c.2256C>A | XP_011519945.1:p.Leu752= | |
| XM_011521644.1:c.2232C>A | XP_011519946.1:p.Leu744= | |
| XM_011521645.1:c.2163C>A | XP_011519947.1:p.Leu721= | |
| XM_011521640.2:c.2346C>A | XP_011519942.1:p.Leu782= | |
| XM_017022255.1:c.2370C>A | XP_016877744.1:p.Leu790= | |
| XM_017022256.1:c.2328C>A | XP_016877745.1:p.Leu776= | |
| XM_017022257.1:c.2298C>A | XP_016877746.1:p.Leu766= | |
| XM_017022258.1:c.2328C>A | XP_016877747.1:p.Leu776= | |
| XM_017022259.1:c.2256C>A | XP_016877748.1:p.Leu752= | |
| XM_017022260.1:c.2232C>A | XP_016877749.1:p.Leu744= | |
| XM_017022261.1:c.2175C>A | XP_016877750.1:p.Leu725= | |
| XM_017022262.1:c.2268+19738C>A | XP_016877751.1:n.2268+19738C>A | |
| XM_017022263.1:c.2163C>A | XP_016877752.1:p.Leu721= | |
| XM_017022264.1:c.2163C>A | XP_016877753.1:p.Leu721= | |
| NM_000275.3:c.2304C>A MANE Select | NP_000266.2:p.Leu768= | |
| NM_001300984.2:c.2232C>A | NP_001287913.1:p.Leu744= |