Linked Data
ClinVar Variation Id:
141931
dbSNP Id:
rs112610898
ExAC:
5:112176981 A / C
gnomAD v2:
5-112176981-A-C
gnomAD v3:
5-112841284-A-C
gnomAD v4:
5-112841284-A-C
PubMed:
PMID:25980754
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112841284A>C , CM000667.2:g.112841284A>C | GRCh38 |
| NC_000005.9:g.112176981A>C , CM000667.1:g.112176981A>C | GRCh37 |
| NC_000005.8:g.112204880A>C | NCBI36 |
| NG_008481.4:g.153764A>C , LRG_130:g.153764A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5744A>C | ENSP00000473355.2:p.His1915Pro | |
| ENST00000505350.2:c.*5696A>C | ENSP00000481752.1:n.*5696A>C | |
| ENST00000507379.6:c.5636A>C | ENSP00000423224.2:p.His1879Pro | |
| ENST00000509732.6:c.5690A>C | ENSP00000426541.2:p.His1897Pro | |
| ENST00000512211.7:c.5690A>C | ENSP00000423828.3:p.His1897Pro | |
| ENST00000257430.9:c.5690A>C MANE Select | ENSP00000257430.4:p.His1897Pro | |
| ENST00000257430.8:c.5690A>C | ENSP00000257430.4:p.His1897Pro | |
| ENST00000508376.6:c.5690A>C | ENSP00000427089.2:p.His1897Pro | |
| ENST00000508624.5:c.*5012A>C | ENSP00000424265.1:n.*5012A>C | |
| ENST00000520401.1:c.230+12312A>C | ||
| NM_000038.5:c.5690A>C | NP_000029.2:p.His1897Pro | |
| NM_001127510.2:c.5690A>C | NP_001120982.1:p.His1897Pro | |
| NM_001127511.2:c.5636A>C | NP_001120983.2:p.His1879Pro | |
| NM_001354895.1:c.5690A>C | NP_001341824.1:p.His1897Pro | |
| NM_001354896.1:c.5744A>C | NP_001341825.1:p.His1915Pro | |
| NM_001354897.1:c.5720A>C | NP_001341826.1:p.His1907Pro | |
| NM_001354898.1:c.5615A>C | NP_001341827.1:p.His1872Pro | |
| NM_001354899.1:c.5606A>C | NP_001341828.1:p.His1869Pro | |
| NM_001354900.1:c.5567A>C | NP_001341829.1:p.His1856Pro | |
| NM_001354901.1:c.5513A>C | NP_001341830.1:p.His1838Pro | |
| NM_001354902.1:c.5417A>C | NP_001341831.1:p.His1806Pro | |
| NM_001354903.1:c.5387A>C | NP_001341832.1:p.His1796Pro | |
| NM_001354904.1:c.5312A>C | NP_001341833.1:p.His1771Pro | |
| NM_001354905.1:c.5210A>C | NP_001341834.1:p.His1737Pro | |
| NM_001354906.1:c.4841A>C | NP_001341835.1:p.His1614Pro | |
| NM_000038.6:c.5690A>C MANE Select | NP_000029.2:p.His1897Pro | |
| NM_001127510.3:c.5690A>C | NP_001120982.1:p.His1897Pro | |
| NM_001127511.3:c.5636A>C | NP_001120983.2:p.His1879Pro | |
| NM_001354895.2:c.5690A>C | NP_001341824.1:p.His1897Pro | |
| NM_001354896.2:c.5744A>C | NP_001341825.1:p.His1915Pro | |
| NM_001354897.2:c.5720A>C | NP_001341826.1:p.His1907Pro | |
| NM_001354898.2:c.5615A>C | NP_001341827.1:p.His1872Pro | |
| NM_001354899.2:c.5606A>C | NP_001341828.1:p.His1869Pro | |
| NM_001354900.2:c.5567A>C | NP_001341829.1:p.His1856Pro | |
| NM_001354901.2:c.5513A>C | NP_001341830.1:p.His1838Pro | |
| NM_001354902.2:c.5417A>C | NP_001341831.1:p.His1806Pro | |
| NM_001354903.2:c.5387A>C | NP_001341832.1:p.His1796Pro | |
| NM_001354904.2:c.5312A>C | NP_001341833.1:p.His1771Pro | |
| NM_001354905.2:c.5210A>C | NP_001341834.1:p.His1737Pro | |
| NM_001354906.2:c.4841A>C | NP_001341835.1:p.His1614Pro |