Linked Data
ClinVar Variation Id:
951646
ClinVar RCV Id:
RCV001223608
dbSNP Id:
rs760315494
ExAC:
16:68867309 G / T
gnomAD v2:
16-68867309-G-T
gnomAD v4:
16-68833406-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68833406G>T , CM000678.2:g.68833406G>T | GRCh38 |
| NC_000016.9:g.68867309G>T , CM000678.1:g.68867309G>T | GRCh37 |
| NC_000016.8:g.67424810G>T | NCBI36 |
| NG_008021.1:g.101115G>T , LRG_301:g.101115G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.2556G>T MANE Select | ENSP00000261769.4:p.Glu852Asp | |
| ENST00000261769.9:c.2556G>T | ENSP00000261769.4:p.Glu852Asp | |
| ENST00000422392.6:c.2373G>T | ENSP00000414946.2:p.Glu791Asp | |
| ENST00000562118.1:n.774G>T | ||
| ENST00000562836.5:n.2627G>T | ||
| ENST00000566510.5:c.*1222G>T | ENSP00000458139.1:n.*1222G>T | |
| ENST00000566612.5:c.*796G>T | ENSP00000454782.1:n.*796G>T | |
| ENST00000611625.4:c.2619G>T | ENSP00000481063.1:p.Glu873Asp | |
| ENST00000612417.4:c.1854-785G>T | ENSP00000478360.1:n.1854-785G>T | |
| ENST00000621016.4:c.1866-797G>T | ENSP00000480664.1:n.1866-797G>T | |
| NM_004360.3:c.2556G>T , LRG_301t1:c.2556G>T | NP_004351.1:p.Glu852Asp | |
| XM_011523488.1:c.1821G>T | XP_011521790.1:p.Glu607Asp | |
| XM_011523489.1:c.1821G>T | XP_011521791.1:p.Glu607Asp | |
| NM_001317184.1:c.2373G>T | NP_001304113.1:p.Glu791Asp | |
| NM_001317185.1:c.1008G>T | NP_001304114.1:p.Glu336Asp | |
| NM_001317186.1:c.591G>T | NP_001304115.1:p.Glu197Asp | |
| NM_004360.4:c.2556G>T | NP_004351.1:p.Glu852Asp | |
| NM_004360.5:c.2556G>T MANE Select | NP_004351.1:p.Glu852Asp | |
| NM_001317184.2:c.2373G>T | NP_001304113.1:p.Glu791Asp | |
| NM_001317185.2:c.1008G>T | NP_001304114.1:p.Glu336Asp | |
| NM_001317186.2:c.591G>T | NP_001304115.1:p.Glu197Asp |