Linked Data
dbSNP Id:
rs753914355
ExAC:
10:61905734 G / A
gnomAD v2:
10-61905734-G-A
gnomAD v3:
10-60145976-G-A
gnomAD v4:
10-60145976-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.60145976G>A , CM000672.2:g.60145976G>A | GRCh38 |
| NC_000010.10:g.61905734G>A , CM000672.1:g.61905734G>A | GRCh37 |
| NC_000010.9:g.61575740G>A | NCBI36 |
| NG_029917.1:g.592551C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000467420.7:c.2576-6889C>T | ENSP00000423968.2:n.2576-6889C>T | |
| ENST00000503366.6:c.2609C>T | ENSP00000425236.1:p.Thr870Met | |
| ENST00000280772.7:c.2615-6889C>T MANE Select | ENSP00000280772.1:n.2615-6889C>T | |
| ENST00000280772.6:c.2615-6889C>T | ENSP00000280772.1:n.2615-6889C>T | |
| ENST00000373827.6:c.2597-6889C>T | ENSP00000362933.2:n.2597-6889C>T | |
| ENST00000460468.5:c.98C>T | ENSP00000426690.1:p.Thr33Met | |
| ENST00000474360.1:c.182C>T | ENSP00000422657.1:p.Thr61Met | |
| ENST00000503366.5:c.2609C>T | ENSP00000425236.1:p.Thr870Met | |
| ENST00000622427.4:c.*1184-6889C>T | ENSP00000483244.1:n.*1184-6889C>T | |
| NM_001204403.1:c.2597-6889C>T | NP_001191332.1:n.2597-6889C>T | |
| NM_001204404.1:c.2609C>T | NP_001191333.1:p.Thr870Met | |
| NM_020987.3:c.2615-6889C>T | NP_066267.2:n.2615-6889C>T | |
| XM_005269715.2:c.2660C>T | XP_005269772.1:p.Thr887Met | |
| XM_005269716.2:c.2615-6889C>T | XP_005269773.1:n.2615-6889C>T | |
| XM_006717791.2:c.2660C>T | XP_006717854.1:p.Thr887Met | |
| XM_006717793.2:c.2660C>T | XP_006717856.1:p.Thr887Met | |
| XM_006717795.2:c.2660C>T | XP_006717858.1:p.Thr887Met | |
| XM_006717796.2:c.2660C>T | XP_006717859.1:p.Thr887Met | |
| XM_006717802.2:c.2660C>T | XP_006717865.1:p.Thr887Met | |
| XM_011539700.1:c.2648C>T | XP_011538002.1:p.Thr883Met | |
| XM_011539701.1:c.2642C>T | XP_011538003.1:p.Thr881Met | |
| XM_011539702.1:c.2603C>T | XP_011538004.1:p.Thr868Met | |
| XM_011539703.1:c.2582C>T | XP_011538005.1:p.Thr861Met | |
| XM_011539704.1:c.2561C>T | XP_011538006.1:p.Thr854Met | |
| XM_011539705.1:c.2561C>T | XP_011538007.1:p.Thr854Met | |
| XM_011539706.1:c.2549C>T | XP_011538008.1:p.Thr850Met | |
| XM_011539707.1:c.2660C>T | XP_011538009.1:p.Thr887Met | |
| XM_011539708.1:c.2660C>T | XP_011538010.1:p.Thr887Met | |
| XM_011539709.1:c.2660C>T | XP_011538011.1:p.Thr887Met | |
| XM_011539710.1:c.2660C>T | XP_011538012.1:p.Thr887Met | |
| XM_011539711.1:c.2660C>T | XP_011538013.1:p.Thr887Met | |
| XM_011539712.1:c.2660C>T | XP_011538014.1:p.Thr887Met | |
| XM_011539713.1:c.2660C>T | XP_011538015.1:p.Thr887Met | |
| XM_011539716.1:c.2660C>T | XP_011538018.1:p.Thr887Met | |
| XM_011539717.1:c.2660C>T | XP_011538019.1:p.Thr887Met | |
| XM_011539718.1:c.2552-6889C>T | XP_011538020.1:n.2552-6889C>T | |
| XM_011539719.1:c.2660C>T | XP_011538021.1:p.Thr887Met | |
| NM_001320874.1:c.2615-6889C>T | NP_001307803.1:n.2615-6889C>T | |
| NM_020987.4:c.2615-6889C>T | NP_066267.2:n.2615-6889C>T | |
| XM_005269715.3:c.2660C>T | XP_005269772.1:p.Thr887Met | |
| XM_006717796.3:c.2660C>T | XP_006717859.1:p.Thr887Met | |
| XM_006717802.3:c.2660C>T | XP_006717865.1:p.Thr887Met | |
| XM_011539708.2:c.2660C>T | XP_011538010.1:p.Thr887Met | |
| XM_011539709.2:c.2660C>T | XP_011538011.1:p.Thr887Met | |
| XM_017016110.1:c.2660C>T | XP_016871599.1:p.Thr887Met | |
| XM_017016111.1:c.2660C>T | XP_016871600.1:p.Thr887Met | |
| XM_017016112.1:c.2660C>T | XP_016871601.1:p.Thr887Met | |
| XM_017016113.1:c.2660C>T | XP_016871602.1:p.Thr887Met | |
| XM_017016114.1:c.2609C>T | XP_016871603.1:p.Thr870Met | |
| XM_017016115.1:c.2582C>T | XP_016871604.1:p.Thr861Met | |
| XM_017016116.1:c.2660C>T | XP_016871605.1:p.Thr887Met | |
| XM_017016117.1:c.2660C>T | XP_016871606.1:p.Thr887Met | |
| XM_017016118.1:c.2660C>T | XP_016871607.1:p.Thr887Met | |
| XM_017016119.1:c.2660C>T | XP_016871608.1:p.Thr887Met | |
| XM_017016120.1:c.2660C>T | XP_016871609.1:p.Thr887Met | |
| XM_017016121.1:c.2660C>T | XP_016871610.1:p.Thr887Met | |
| XM_017016122.1:c.2615-6889C>T | XP_016871611.1:n.2615-6889C>T | |
| XM_017016123.1:c.2660C>T | XP_016871612.1:p.Thr887Met | |
| XM_017016124.1:c.2660C>T | XP_016871613.1:p.Thr887Met | |
| XM_017016125.1:c.2660C>T | XP_016871614.1:p.Thr887Met | |
| XM_017016126.1:c.2552-6889C>T | XP_016871615.1:n.2552-6889C>T | |
| XM_017016127.1:c.2552-6889C>T | XP_016871616.1:n.2552-6889C>T | |
| XM_017016128.1:c.2660C>T | XP_016871617.1:p.Thr887Met | |
| XM_017016129.1:c.2660C>T | XP_016871618.1:p.Thr887Met | |
| XM_017016130.1:c.2615-6889C>T | XP_016871619.1:n.2615-6889C>T | |
| XM_017016131.1:c.2615-6889C>T | XP_016871620.1:n.2615-6889C>T | |
| XM_017016132.1:c.2615-6889C>T | XP_016871621.1:n.2615-6889C>T | |
| XM_017016134.1:c.2552-6889C>T | XP_016871623.1:n.2552-6889C>T | |
| XM_017016136.1:c.2660C>T | XP_016871625.1:p.Thr887Met | |
| XM_017016137.1:c.2660C>T | XP_016871626.1:p.Thr887Met | |
| XM_017016138.1:c.2660C>T | XP_016871627.1:p.Thr887Met | |
| XM_017016141.1:c.2552-6889C>T | XP_016871630.1:n.2552-6889C>T | |
| XM_024447953.1:c.2660C>T | XP_024303721.1:p.Thr887Met | |
| XM_024447954.1:c.2615-6889C>T | XP_024303722.1:n.2615-6889C>T | |
| XM_024447955.1:c.2597C>T | XP_024303723.1:p.Thr866Met | |
| XM_024447956.1:c.2615-6889C>T | XP_024303724.1:n.2615-6889C>T | |
| XM_024447957.1:c.2561C>T | XP_024303725.1:p.Thr854Met | |
| XM_024447958.1:c.2564-6889C>T | XP_024303726.1:n.2564-6889C>T | |
| XM_024447959.1:c.2552-6889C>T | XP_024303727.1:n.2552-6889C>T | |
| XM_024447960.1:c.2552-6889C>T | XP_024303728.1:n.2552-6889C>T | |
| XM_024447961.1:c.2552-6889C>T | XP_024303729.1:n.2552-6889C>T | |
| XM_024447962.1:c.2660C>T | XP_024303730.1:p.Thr887Met | |
| XM_024447963.1:c.2660C>T | XP_024303731.1:p.Thr887Met | |
| XM_024447964.1:c.2660C>T | XP_024303732.1:p.Thr887Met | |
| XM_024447965.1:c.2660C>T | XP_024303733.1:p.Thr887Met | |
| NM_020987.5:c.2615-6889C>T MANE Select | NP_066267.2:n.2615-6889C>T | |
| NM_001204403.2:c.2597-6889C>T | NP_001191332.1:n.2597-6889C>T | |
| NM_001204404.2:c.2609C>T | NP_001191333.1:p.Thr870Met | |
| NM_001320874.2:c.2615-6889C>T | NP_001307803.1:n.2615-6889C>T |