Linked Data
ClinVar Variation Id:
210553
dbSNP Id:
rs141911199
ExAC:
5:37183766 T / C
gnomAD v2:
5-37183766-T-C
gnomAD v3:
5-37183664-T-C
gnomAD v4:
5-37183664-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37183664T>C , CM000667.2:g.37183664T>C | GRCh38 |
| NC_000005.9:g.37183766T>C , CM000667.1:g.37183766T>C | GRCh37 |
| NC_000005.8:g.37219523T>C | NCBI36 |
| NG_032772.1:g.70765A>G | |
| NG_032772.2:g.70765A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425232.7:c.4021A>G | ||
| ENST00000651892.2:c.4517A>G MANE Select | ENSP00000498265.2:p.His1506Arg | |
| ENST00000425232.6:c.4517A>G | ENSP00000389014.2:p.His1506Arg | |
| ENST00000508244.5:c.4517A>G | ENSP00000421690.1:p.His1506Arg | |
| ENST00000509849.5:c.1532A>G | ENSP00000426337.1:p.His511Arg | |
| ENST00000514429.5:c.1661A>G | ENSP00000424223.1:p.His554Arg | |
| NM_023073.3:c.4517A>G | NP_075561.3:p.His1506Arg | |
| XM_005248345.2:c.4517A>G | XP_005248402.1:p.His1506Arg | |
| XM_005248346.2:c.4517A>G | XP_005248403.1:p.His1506Arg | |
| XM_005248347.2:c.4517A>G | XP_005248404.1:p.His1506Arg | |
| XM_005248349.2:c.4517A>G | XP_005248406.1:p.His1506Arg | |
| XM_005248350.2:c.4388A>G | XP_005248407.1:p.His1463Arg | |
| XM_005248353.3:c.1160A>G | XP_005248410.1:p.His387Arg | |
| XM_006714489.2:c.4517A>G | XP_006714552.1:p.His1506Arg | |
| XM_011514085.1:c.4517A>G | XP_011512387.1:p.His1506Arg | |
| XM_011514086.1:c.4517A>G | XP_011512388.1:p.His1506Arg | |
| XM_011514087.1:c.4517A>G | XP_011512389.1:p.His1506Arg | |
| XM_011514088.1:c.4517A>G | XP_011512390.1:p.His1506Arg | |
| XM_011514089.1:c.4517A>G | XP_011512391.1:p.His1506Arg | |
| XM_011514090.1:c.4199A>G | XP_011512392.1:p.His1400Arg | |
| XM_011514091.1:c.3845A>G | XP_011512393.1:p.His1282Arg | |
| XM_011514092.1:c.4517A>G | XP_011512394.1:p.His1506Arg | |
| XM_011514093.1:c.4517A>G | XP_011512395.1:p.His1506Arg | |
| XM_011514094.1:c.1742A>G | XP_011512396.1:p.His581Arg | |
| XR_427661.2:n.4692A>G | ||
| XR_925644.1:n.4692A>G | ||
| XM_005248345.4:c.4517A>G | XP_005248402.1:p.His1506Arg | |
| XM_005248346.4:c.4517A>G | XP_005248403.1:p.His1506Arg | |
| XM_005248347.4:c.4517A>G | XP_005248404.1:p.His1506Arg | |
| XM_005248349.4:c.4517A>G | XP_005248406.1:p.His1506Arg | |
| XM_005248350.4:c.4388A>G | XP_005248407.1:p.His1463Arg | |
| XM_011514085.3:c.4517A>G | XP_011512387.1:p.His1506Arg | |
| XM_011514086.3:c.4517A>G | XP_011512388.1:p.His1506Arg | |
| XM_011514087.2:c.4517A>G | XP_011512389.1:p.His1506Arg | |
| XM_011514088.2:c.4517A>G | XP_011512390.1:p.His1506Arg | |
| XM_011514089.2:c.4517A>G | XP_011512391.1:p.His1506Arg | |
| XM_011514090.3:c.4199A>G | XP_011512392.1:p.His1400Arg | |
| XM_011514092.2:c.4517A>G | XP_011512394.1:p.His1506Arg | |
| XM_011514094.2:c.1742A>G | XP_011512396.1:p.His581Arg | |
| XM_017009760.1:c.4328A>G | XP_016865249.1:p.His1443Arg | |
| XM_017009761.2:c.4328A>G | XP_016865250.1:p.His1443Arg | |
| XM_017009763.1:c.3524A>G | XP_016865252.1:p.His1175Arg | |
| XM_017009765.1:c.3329A>G | XP_016865254.1:p.His1110Arg | |
| XM_017009766.1:c.1160A>G | XP_016865255.1:p.His387Arg | |
| XM_024446183.1:c.4328A>G | XP_024301951.1:p.His1443Arg | |
| XM_024446184.1:c.4199A>G | XP_024301952.1:p.His1400Arg | |
| XM_024446185.1:c.3845A>G | XP_024301953.1:p.His1282Arg | |
| XM_024446186.1:c.3524A>G | XP_024301954.1:p.His1175Arg | |
| XR_001742208.1:n.4741A>G | ||
| XR_002956171.1:n.4741A>G | ||
| XR_925644.2:n.4741A>G | ||
| NM_001384732.1:c.4517A>G MANE Select | NP_001371661.1:p.His1506Arg | |
| NM_023073.4:c.4517A>G | NP_075561.3:p.His1506Arg |