Linked Data
ClinVar Variation Id:
283021
dbSNP Id:
rs201548223
ExAC:
6:152469439 G / C
gnomAD v2:
6-152469439-G-C
gnomAD v3:
6-152148304-G-C
gnomAD v4:
6-152148304-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152148304G>C , CM000668.2:g.152148304G>C | GRCh38 |
| NC_000006.11:g.152469439G>C , CM000668.1:g.152469439G>C | GRCh37 |
| NC_000006.10:g.152511132G>C | NCBI36 |
| NG_012855.1:g.494096C>G | |
| NG_012855.2:g.494096C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1182C>G MANE Plus Clinical | ENSP00000346701.4:p.His394Gln | |
| ENST00000367255.10:c.24717C>G MANE Select | ENSP00000356224.5:p.His8239Gln | |
| ENST00000423061.6:c.24504C>G | ENSP00000396024.1:p.His8168Gln | |
| ENST00000672154.1:c.159-40C>G | ||
| ENST00000672169.1:c.452C>G | ||
| ENST00000673173.1:c.631C>G | ||
| ENST00000673451.1:c.489C>G | ENSP00000500189.1:p.His163Gln | |
| ENST00000341594.9:c.23502C>G | ENSP00000341887.6:p.His7834Gln | |
| ENST00000347037.9:n.1396C>G | ||
| ENST00000354674.4:c.1182C>G | ENSP00000346701.4:p.His394Gln | |
| ENST00000367251.7:c.3483C>G | ENSP00000356220.3:p.His1161Gln | |
| ENST00000367255.9:c.24717C>G | ENSP00000356224.5:p.His8239Gln | |
| ENST00000367256.9:n.8409C>G | ||
| ENST00000367257.8:c.2655C>G | ENSP00000356226.4:p.His885Gln | |
| ENST00000409694.6:n.8301C>G | ||
| ENST00000423061.5:c.24504C>G | ENSP00000396024.1:p.His8168Gln | |
| ENST00000460912.6:n.1262C>G | ||
| ENST00000472563.2:n.105C>G | ||
| ENST00000536990.5:n.1554C>G | ||
| ENST00000539504.5:c.1182C>G | ENSP00000441052.1:p.His394Gln | |
| NM_033071.3:c.24504C>G | NP_149062.1:p.His8168Gln | |
| NM_182961.3:c.24717C>G | NP_892006.3:p.His8239Gln | |
| XM_006715407.1:c.24753C>G | XP_006715470.1:p.His8251Gln | |
| XM_006715408.1:c.24741C>G | XP_006715471.1:p.His8247Gln | |
| XM_006715409.1:c.24732C>G | XP_006715472.1:p.His8244Gln | |
| XM_006715410.1:c.24753C>G | XP_006715473.1:p.His8251Gln | |
| XM_006715411.1:c.24702C>G | XP_006715474.1:p.His8234Gln | |
| XM_006715412.1:c.24738C>G | XP_006715475.1:p.His8246Gln | |
| XM_006715413.1:c.24753C>G | XP_006715476.1:p.His8251Gln | |
| XM_006715414.1:c.24681C>G | XP_006715477.1:p.His8227Gln | |
| XM_006715415.1:c.24753C>G | XP_006715478.1:p.His8251Gln | |
| XM_006715416.1:c.24738C>G | XP_006715479.1:p.His8246Gln | |
| XM_006715417.1:c.24612C>G | XP_006715480.1:p.His8204Gln | |
| XM_006715420.1:c.24600C>G | XP_006715483.1:p.His8200Gln | |
| XM_006715421.1:c.24597C>G | XP_006715484.1:p.His8199Gln | |
| XM_006715422.1:c.24594C>G | XP_006715485.1:p.His8198Gln | |
| XM_006715423.1:c.24753C>G | XP_006715486.1:p.His8251Gln | |
| XM_006715424.1:c.24753C>G | XP_006715487.1:p.His8251Gln | |
| XM_006715425.1:c.24753C>G | XP_006715488.1:p.His8251Gln | |
| XM_011535641.1:c.24750C>G | XP_011533943.1:p.His8250Gln | |
| XM_011535642.1:c.24738C>G | XP_011533944.1:p.His8246Gln | |
| XM_011535643.1:c.24588C>G | XP_011533945.1:p.His8196Gln | |
| XM_011535644.1:c.23028C>G | XP_011533946.1:p.His7676Gln | |
| XM_011535645.1:c.22521C>G | XP_011533947.1:p.His7507Gln | |
| XM_011535647.1:c.17988C>G | XP_011533949.1:p.His5996Gln | |
| NM_001347701.1:c.1323C>G | NP_001334630.1:p.His441Gln | |
| NM_001347702.1:c.1182C>G | NP_001334631.1:p.His394Gln | |
| XM_006715408.2:c.24741C>G | XP_006715471.1:p.His8247Gln | |
| XM_006715410.2:c.24753C>G | XP_006715473.1:p.His8251Gln | |
| XM_006715412.2:c.24738C>G | XP_006715475.1:p.His8246Gln | |
| XM_006715413.2:c.24753C>G | XP_006715476.1:p.His8251Gln | |
| XM_006715415.2:c.24753C>G | XP_006715478.1:p.His8251Gln | |
| XM_006715416.2:c.24738C>G | XP_006715479.1:p.His8246Gln | |
| XM_006715417.2:c.24612C>G | XP_006715480.1:p.His8204Gln | |
| XM_006715420.2:c.24600C>G | XP_006715483.1:p.His8200Gln | |
| XM_006715421.2:c.24597C>G | XP_006715484.1:p.His8199Gln | |
| XM_006715423.2:c.24753C>G | XP_006715486.1:p.His8251Gln | |
| XM_006715424.2:c.24753C>G | XP_006715487.1:p.His8251Gln | |
| XM_006715425.2:c.24753C>G | XP_006715488.1:p.His8251Gln | |
| XM_011535641.2:c.24750C>G | XP_011533943.1:p.His8250Gln | |
| XM_011535642.2:c.24738C>G | XP_011533944.1:p.His8246Gln | |
| XM_011535645.2:c.22521C>G | XP_011533947.1:p.His7507Gln | |
| XM_017010608.1:c.24753C>G | XP_016866097.1:p.His8251Gln | |
| XM_017010609.1:c.24753C>G | XP_016866098.1:p.His8251Gln | |
| XM_017010610.1:c.24732C>G | XP_016866099.1:p.His8244Gln | |
| XM_017010611.2:c.24726C>G | XP_016866100.1:p.His8242Gln | |
| XM_017010612.1:c.24675C>G | XP_016866101.1:p.His8225Gln | |
| XM_017010613.1:c.24750C>G | XP_016866102.1:p.His8250Gln | |
| XM_017010614.1:c.24597C>G | XP_016866103.1:p.His8199Gln | |
| XM_017010615.1:c.24597C>G | XP_016866104.1:p.His8199Gln | |
| XM_017010616.1:c.24753C>G | XP_016866105.1:p.His8251Gln | |
| XM_017010617.1:c.24750C>G | XP_016866106.1:p.His8250Gln | |
| XM_017010618.1:c.24738C>G | XP_016866107.1:p.His8246Gln | |
| XM_017010619.1:c.23028C>G | XP_016866108.1:p.His7676Gln | |
| NM_182961.4:c.24717C>G MANE Select | NP_892006.3:p.His8239Gln | |
| NM_001347701.2:c.1323C>G | NP_001334630.1:p.His441Gln | |
| NM_001347702.2:c.1182C>G MANE Plus Clinical | NP_001334631.1:p.His394Gln | |
| NM_033071.5:c.24504C>G | NP_149062.2:p.His8168Gln |