Linked Data
ClinVar Variation Id:
481704
dbSNP Id:
rs113583899
gnomAD v3:
16-68819279-G-C
gnomAD v4:
16-68819279-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68819279G>C , CM000678.2:g.68819279G>C | GRCh38 |
| NC_000016.9:g.68853182G>C , CM000678.1:g.68853182G>C | GRCh37 |
| NC_000016.8:g.67410683G>C | NCBI36 |
| NG_008021.1:g.86988G>C , LRG_301:g.86988G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.1566-1G>C MANE Select | ENSP00000261769.4:n.1566-1G>C | |
| ENST00000261769.9:c.1566-1G>C | ENSP00000261769.4:n.1566-1G>C | |
| ENST00000422392.6:c.1383-1G>C | ENSP00000414946.2:n.1383-1G>C | |
| ENST00000562836.5:n.1637-1G>C | ||
| ENST00000566510.5:c.*232-1G>C | ENSP00000458139.1:n.*232-1G>C | |
| ENST00000566612.5:c.1566-2722G>C | ENSP00000454782.1:n.1566-2722G>C | |
| ENST00000611625.4:c.1629-1G>C | ENSP00000481063.1:n.1629-1G>C | |
| ENST00000612417.4:c.1566-1G>C | ENSP00000478360.1:n.1566-1G>C | |
| ENST00000621016.4:c.1566-1G>C | ENSP00000480664.1:n.1566-1G>C | |
| NM_004360.3:c.1566-1G>C , LRG_301t1:c.1566-1G>C | NP_004351.1:n.1566-1G>C | |
| XM_011523488.1:c.831-1G>C | XP_011521790.1:n.831-1G>C | |
| XM_011523489.1:c.831-1G>C | XP_011521791.1:n.831-1G>C | |
| NM_001317184.1:c.1383-1G>C | NP_001304113.1:n.1383-1G>C | |
| NM_001317185.1:c.18-1G>C | NP_001304114.1:n.18-1G>C | |
| NM_001317186.1:c.-254-2722G>C | NP_001304115.1:n.-254-2722G>C | |
| NM_004360.4:c.1566-1G>C | NP_004351.1:n.1566-1G>C | |
| NM_004360.5:c.1566-1G>C MANE Select | NP_004351.1:n.1566-1G>C | |
| NM_001317184.2:c.1383-1G>C | NP_001304113.1:n.1383-1G>C | |
| NM_001317185.2:c.18-1G>C | NP_001304114.1:n.18-1G>C | |
| NM_001317186.2:c.-254-2722G>C | NP_001304115.1:n.-254-2722G>C |