Linked Data
ClinVar Variation Id:
219895
dbSNP Id:
rs750012595
ExAC:
5:112178868 A / G
gnomAD v2:
5-112178868-A-G
gnomAD v4:
5-112843171-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112843171A>G , CM000667.2:g.112843171A>G | GRCh38 |
| NC_000005.9:g.112178868A>G , CM000667.1:g.112178868A>G | GRCh37 |
| NC_000005.8:g.112206767A>G | NCBI36 |
| NG_008481.4:g.155651A>G , LRG_130:g.155651A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7631A>G | ENSP00000473355.2:p.His2544Arg | |
| ENST00000505350.2:c.*7583A>G | ENSP00000481752.1:n.*7583A>G | |
| ENST00000507379.6:c.7523A>G | ENSP00000423224.2:p.His2508Arg | |
| ENST00000509732.6:c.7577A>G | ENSP00000426541.2:p.His2526Arg | |
| ENST00000512211.7:c.7577A>G | ENSP00000423828.3:p.His2526Arg | |
| ENST00000257430.9:c.7577A>G MANE Select | ENSP00000257430.4:p.His2526Arg | |
| ENST00000257430.8:c.7577A>G | ENSP00000257430.4:p.His2526Arg | |
| ENST00000508376.6:c.7577A>G | ENSP00000427089.2:p.His2526Arg | |
| ENST00000520401.1:c.231-13478A>G | ||
| NM_000038.5:c.7577A>G | NP_000029.2:p.His2526Arg | |
| NM_001127510.2:c.7577A>G | NP_001120982.1:p.His2526Arg | |
| NM_001127511.2:c.7523A>G | NP_001120983.2:p.His2508Arg | |
| NM_001354895.1:c.7577A>G | NP_001341824.1:p.His2526Arg | |
| NM_001354896.1:c.7631A>G | NP_001341825.1:p.His2544Arg | |
| NM_001354897.1:c.7607A>G | NP_001341826.1:p.His2536Arg | |
| NM_001354898.1:c.7502A>G | NP_001341827.1:p.His2501Arg | |
| NM_001354899.1:c.7493A>G | NP_001341828.1:p.His2498Arg | |
| NM_001354900.1:c.7454A>G | NP_001341829.1:p.His2485Arg | |
| NM_001354901.1:c.7400A>G | NP_001341830.1:p.His2467Arg | |
| NM_001354902.1:c.7304A>G | NP_001341831.1:p.His2435Arg | |
| NM_001354903.1:c.7274A>G | NP_001341832.1:p.His2425Arg | |
| NM_001354904.1:c.7199A>G | NP_001341833.1:p.His2400Arg | |
| NM_001354905.1:c.7097A>G | NP_001341834.1:p.His2366Arg | |
| NM_001354906.1:c.6728A>G | NP_001341835.1:p.His2243Arg | |
| NM_000038.6:c.7577A>G MANE Select | NP_000029.2:p.His2526Arg | |
| NM_001127510.3:c.7577A>G | NP_001120982.1:p.His2526Arg | |
| NM_001127511.3:c.7523A>G | NP_001120983.2:p.His2508Arg | |
| NM_001354895.2:c.7577A>G | NP_001341824.1:p.His2526Arg | |
| NM_001354896.2:c.7631A>G | NP_001341825.1:p.His2544Arg | |
| NM_001354897.2:c.7607A>G | NP_001341826.1:p.His2536Arg | |
| NM_001354898.2:c.7502A>G | NP_001341827.1:p.His2501Arg | |
| NM_001354899.2:c.7493A>G | NP_001341828.1:p.His2498Arg | |
| NM_001354900.2:c.7454A>G | NP_001341829.1:p.His2485Arg | |
| NM_001354901.2:c.7400A>G | NP_001341830.1:p.His2467Arg | |
| NM_001354902.2:c.7304A>G | NP_001341831.1:p.His2435Arg | |
| NM_001354903.2:c.7274A>G | NP_001341832.1:p.His2425Arg | |
| NM_001354904.2:c.7199A>G | NP_001341833.1:p.His2400Arg | |
| NM_001354905.2:c.7097A>G | NP_001341834.1:p.His2366Arg | |
| NM_001354906.2:c.6728A>G | NP_001341835.1:p.His2243Arg |