Linked Data
ClinVar Variation Id:
500171
dbSNP Id:
rs761266231
ExAC:
6:152466677 G / A
gnomAD v2:
6-152466677-G-A
gnomAD v3:
6-152145542-G-A
gnomAD v4:
6-152145542-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152145542G>A , CM000668.2:g.152145542G>A | GRCh38 |
| NC_000006.11:g.152466677G>A , CM000668.1:g.152466677G>A | GRCh37 |
| NC_000006.10:g.152508370G>A | NCBI36 |
| NG_012855.1:g.496858C>T | |
| NG_012855.2:g.496858C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1455C>T MANE Plus Clinical | ENSP00000346701.4:p.Pro485= | |
| ENST00000367255.10:c.24977-1777C>T MANE Select | ENSP00000356224.5:n.24977-1777C>T | |
| ENST00000423061.6:c.24777C>T | ENSP00000396024.1:p.Pro8259= | |
| ENST00000672154.1:c.379-1777C>T | ||
| ENST00000672169.1:c.712-1777C>T | ||
| ENST00000673173.1:c.890+2503C>T | ||
| ENST00000673451.1:c.749-1777C>T | ENSP00000500189.1:n.749-1777C>T | |
| ENST00000341594.9:c.23762-1777C>T | ENSP00000341887.6:n.23762-1777C>T | |
| ENST00000347037.9:n.1669C>T | ||
| ENST00000354674.4:c.1455C>T | ENSP00000346701.4:p.Pro485= | |
| ENST00000367251.7:c.3756C>T | ENSP00000356220.3:p.Pro1252= | |
| ENST00000367255.9:c.24977-1777C>T | ENSP00000356224.5:n.24977-1777C>T | |
| ENST00000367256.9:n.8669-1777C>T | ||
| ENST00000367257.8:c.2915-1777C>T | ENSP00000356226.4:n.2915-1777C>T | |
| ENST00000409694.6:n.8561-1777C>T | ||
| ENST00000423061.5:c.24777C>T | ENSP00000396024.1:p.Pro8259= | |
| ENST00000460912.6:n.1535C>T | ||
| ENST00000478916.5:n.2222C>T | ||
| ENST00000536990.5:n.1814-1777C>T | ||
| ENST00000539504.5:c.1442-1777C>T | ENSP00000441052.1:n.1442-1777C>T | |
| NM_033071.3:c.24777C>T | NP_149062.1:p.Pro8259= | |
| NM_182961.3:c.24977-1777C>T | NP_892006.3:n.24977-1777C>T | |
| XM_006715407.1:c.25026C>T | XP_006715470.1:p.Pro8342= | |
| XM_006715408.1:c.25014C>T | XP_006715471.1:p.Pro8338= | |
| XM_006715409.1:c.25005C>T | XP_006715472.1:p.Pro8335= | |
| XM_006715410.1:c.25026C>T | XP_006715473.1:p.Pro8342= | |
| XM_006715411.1:c.24975C>T | XP_006715474.1:p.Pro8325= | |
| XM_006715412.1:c.25011C>T | XP_006715475.1:p.Pro8337= | |
| XM_006715413.1:c.25013-1777C>T | XP_006715476.1:n.25013-1777C>T | |
| XM_006715414.1:c.24954C>T | XP_006715477.1:p.Pro8318= | |
| XM_006715415.1:c.25013-1777C>T | XP_006715478.1:n.25013-1777C>T | |
| XM_006715416.1:c.24998-1777C>T | XP_006715479.1:n.24998-1777C>T | |
| XM_006715417.1:c.24885C>T | XP_006715480.1:p.Pro8295= | |
| XM_006715420.1:c.24873C>T | XP_006715483.1:p.Pro8291= | |
| XM_006715421.1:c.24870C>T | XP_006715484.1:p.Pro8290= | |
| XM_006715422.1:c.24867C>T | XP_006715485.1:p.Pro8289= | |
| XM_006715423.1:c.25026C>T | XP_006715486.1:p.Pro8342= | |
| XM_006715424.1:c.25026C>T | XP_006715487.1:p.Pro8342= | |
| XM_006715425.1:c.25013-1777C>T | XP_006715488.1:n.25013-1777C>T | |
| XM_011535641.1:c.25023C>T | XP_011533943.1:p.Pro8341= | |
| XM_011535642.1:c.25011C>T | XP_011533944.1:p.Pro8337= | |
| XM_011535643.1:c.24861C>T | XP_011533945.1:p.Pro8287= | |
| XM_011535644.1:c.23301C>T | XP_011533946.1:p.Pro7767= | |
| XM_011535645.1:c.22794C>T | XP_011533947.1:p.Pro7598= | |
| XM_011535647.1:c.18261C>T | XP_011533949.1:p.Pro6087= | |
| NM_001347701.1:c.1583-1777C>T | NP_001334630.1:n.1583-1777C>T | |
| NM_001347702.1:c.1455C>T | NP_001334631.1:p.Pro485= | |
| XM_006715408.2:c.25014C>T | XP_006715471.1:p.Pro8338= | |
| XM_006715410.2:c.25026C>T | XP_006715473.1:p.Pro8342= | |
| XM_006715412.2:c.25011C>T | XP_006715475.1:p.Pro8337= | |
| XM_006715413.2:c.25013-1777C>T | XP_006715476.1:n.25013-1777C>T | |
| XM_006715415.2:c.25013-1777C>T | XP_006715478.1:n.25013-1777C>T | |
| XM_006715416.2:c.24998-1777C>T | XP_006715479.1:n.24998-1777C>T | |
| XM_006715417.2:c.24885C>T | XP_006715480.1:p.Pro8295= | |
| XM_006715420.2:c.24873C>T | XP_006715483.1:p.Pro8291= | |
| XM_006715421.2:c.24870C>T | XP_006715484.1:p.Pro8290= | |
| XM_006715423.2:c.25026C>T | XP_006715486.1:p.Pro8342= | |
| XM_006715424.2:c.25026C>T | XP_006715487.1:p.Pro8342= | |
| XM_006715425.2:c.25013-1777C>T | XP_006715488.1:n.25013-1777C>T | |
| XM_011535641.2:c.25023C>T | XP_011533943.1:p.Pro8341= | |
| XM_011535642.2:c.25011C>T | XP_011533944.1:p.Pro8337= | |
| XM_011535645.2:c.22794C>T | XP_011533947.1:p.Pro7598= | |
| XM_017010608.1:c.25026C>T | XP_016866097.1:p.Pro8342= | |
| XM_017010609.1:c.25026C>T | XP_016866098.1:p.Pro8342= | |
| XM_017010610.1:c.25005C>T | XP_016866099.1:p.Pro8335= | |
| XM_017010611.2:c.24999C>T | XP_016866100.1:p.Pro8333= | |
| XM_017010612.1:c.24948C>T | XP_016866101.1:p.Pro8316= | |
| XM_017010613.1:c.25010-1777C>T | XP_016866102.1:n.25010-1777C>T | |
| XM_017010614.1:c.24870C>T | XP_016866103.1:p.Pro8290= | |
| XM_017010615.1:c.24857-1777C>T | XP_016866104.1:n.24857-1777C>T | |
| XM_017010616.1:c.25013-1777C>T | XP_016866105.1:n.25013-1777C>T | |
| XM_017010617.1:c.25010-1777C>T | XP_016866106.1:n.25010-1777C>T | |
| XM_017010618.1:c.24998-1777C>T | XP_016866107.1:n.24998-1777C>T | |
| XM_017010619.1:c.23301C>T | XP_016866108.1:p.Pro7767= | |
| NM_182961.4:c.24977-1777C>T MANE Select | NP_892006.3:n.24977-1777C>T | |
| NM_001347701.2:c.1583-1777C>T | NP_001334630.1:n.1583-1777C>T | |
| NM_001347702.2:c.1455C>T MANE Plus Clinical | NP_001334631.1:p.Pro485= | |
| NM_033071.5:c.24777C>T | NP_149062.2:p.Pro8259= |