Linked Data
ClinVar Variation Id:
288230
dbSNP Id:
rs773325406
ExAC:
15:90196090 T / G
gnomAD v2:
15-90196090-T-G
gnomAD v3:
15-89652859-T-G
gnomAD v4:
15-89652859-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89652859T>G , CM000677.2:g.89652859T>G | GRCh38 |
| NC_000015.9:g.90196090T>G , CM000677.1:g.90196090T>G | GRCh37 |
| NC_000015.8:g.87997094T>G | NCBI36 |
| NG_030338.1:g.7593A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696512.1:c.195A>C | ENSP00000512678.1:p.Pro65= | |
| ENST00000394412.8:c.72A>C MANE Select | ENSP00000377934.3:p.Pro24= | |
| ENST00000394412.7:c.72A>C | ENSP00000377934.3:p.Pro24= | |
| ENST00000445906.1:c.72A>C | ENSP00000395906.1:p.Pro24= | |
| NM_198525.2:c.72A>C | NP_940927.2:p.Pro24= | |
| XM_005254902.2:c.72A>C | XP_005254959.1:p.Pro24= | |
| XM_011521531.1:c.195A>C | XP_011519833.1:p.Pro65= | |
| XM_011521532.1:c.195A>C | XP_011519834.1:p.Pro65= | |
| XM_011521533.1:c.195A>C | XP_011519835.1:p.Pro65= | |
| XM_011521534.1:c.195A>C | XP_011519836.1:p.Pro65= | |
| XM_011521535.1:c.195A>C | XP_011519837.1:p.Pro65= | |
| XM_011521536.1:c.195A>C | XP_011519838.1:p.Pro65= | |
| XM_011521537.1:c.195A>C | XP_011519839.1:p.Pro65= | |
| XM_011521531.2:c.195A>C | XP_011519833.1:p.Pro65= | |
| NM_198525.3:c.72A>C MANE Select | NP_940927.2:p.Pro24= |