Linked Data
ClinVar Variation Id:
485127
dbSNP Id:
rs762572576
ExAC:
5:112174029 A / G
gnomAD v2:
5-112174029-A-G
gnomAD v3:
5-112838332-A-G
gnomAD v4:
5-112838332-A-G
PubMed:
PMID:26933808
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838332A>G , CM000667.2:g.112838332A>G | GRCh38 |
| NC_000005.9:g.112174029A>G , CM000667.1:g.112174029A>G | GRCh37 |
| NC_000005.8:g.112201928A>G | NCBI36 |
| NG_008481.4:g.150812A>G , LRG_130:g.150812A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2403A>G | ENSP00000484935.2:n.2403A>G | |
| ENST00000504915.3:c.2792A>G | ENSP00000473355.2:p.His931Arg | |
| ENST00000505350.2:c.*2744A>G | ENSP00000481752.1:n.*2744A>G | |
| ENST00000507379.6:c.2684A>G | ENSP00000423224.2:p.His895Arg | |
| ENST00000509732.6:c.2738A>G | ENSP00000426541.2:p.His913Arg | |
| ENST00000512211.7:c.2738A>G | ENSP00000423828.3:p.His913Arg | |
| ENST00000257430.9:c.2738A>G MANE Select | ENSP00000257430.4:p.His913Arg | |
| ENST00000257430.8:c.2738A>G | ENSP00000257430.4:p.His913Arg | |
| ENST00000502371.2:c.1091A>G | ||
| ENST00000507379.5:c.2684A>G | ENSP00000423224.1:p.His895Arg | |
| ENST00000508376.6:c.2738A>G | ENSP00000427089.2:p.His913Arg | |
| ENST00000508624.5:c.*2060A>G | ENSP00000424265.1:n.*2060A>G | |
| ENST00000512211.6:c.2738A>G | ENSP00000423828.2:p.His913Arg | |
| ENST00000520401.1:c.230+9360A>G | ||
| NM_000038.5:c.2738A>G | NP_000029.2:p.His913Arg | |
| NM_001127510.2:c.2738A>G | NP_001120982.1:p.His913Arg | |
| NM_001127511.2:c.2684A>G | NP_001120983.2:p.His895Arg | |
| NM_001354895.1:c.2738A>G | NP_001341824.1:p.His913Arg | |
| NM_001354896.1:c.2792A>G | NP_001341825.1:p.His931Arg | |
| NM_001354897.1:c.2768A>G | NP_001341826.1:p.His923Arg | |
| NM_001354898.1:c.2663A>G | NP_001341827.1:p.His888Arg | |
| NM_001354899.1:c.2654A>G | NP_001341828.1:p.His885Arg | |
| NM_001354900.1:c.2615A>G | NP_001341829.1:p.His872Arg | |
| NM_001354901.1:c.2561A>G | NP_001341830.1:p.His854Arg | |
| NM_001354902.1:c.2465A>G | NP_001341831.1:p.His822Arg | |
| NM_001354903.1:c.2435A>G | NP_001341832.1:p.His812Arg | |
| NM_001354904.1:c.2360A>G | NP_001341833.1:p.His787Arg | |
| NM_001354905.1:c.2258A>G | NP_001341834.1:p.His753Arg | |
| NM_001354906.1:c.1889A>G | NP_001341835.1:p.His630Arg | |
| NM_000038.6:c.2738A>G MANE Select | NP_000029.2:p.His913Arg | |
| NM_001127510.3:c.2738A>G | NP_001120982.1:p.His913Arg | |
| NM_001127511.3:c.2684A>G | NP_001120983.2:p.His895Arg | |
| NM_001354895.2:c.2738A>G | NP_001341824.1:p.His913Arg | |
| NM_001354896.2:c.2792A>G | NP_001341825.1:p.His931Arg | |
| NM_001354897.2:c.2768A>G | NP_001341826.1:p.His923Arg | |
| NM_001354898.2:c.2663A>G | NP_001341827.1:p.His888Arg | |
| NM_001354899.2:c.2654A>G | NP_001341828.1:p.His885Arg | |
| NM_001354900.2:c.2615A>G | NP_001341829.1:p.His872Arg | |
| NM_001354901.2:c.2561A>G | NP_001341830.1:p.His854Arg | |
| NM_001354902.2:c.2465A>G | NP_001341831.1:p.His822Arg | |
| NM_001354903.2:c.2435A>G | NP_001341832.1:p.His812Arg | |
| NM_001354904.2:c.2360A>G | NP_001341833.1:p.His787Arg | |
| NM_001354905.2:c.2258A>G | NP_001341834.1:p.His753Arg | |
| NM_001354906.2:c.1889A>G | NP_001341835.1:p.His630Arg |