Linked Data
ClinVar Variation Id:
491504
dbSNP Id:
rs200399144
gnomAD v2:
16-68853204-T-C
gnomAD v3:
16-68819301-T-C
gnomAD v4:
16-68819301-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68819301T>C , CM000678.2:g.68819301T>C | GRCh38 |
| NC_000016.9:g.68853204T>C , CM000678.1:g.68853204T>C | GRCh37 |
| NC_000016.8:g.67410705T>C | NCBI36 |
| NG_008021.1:g.87010T>C , LRG_301:g.87010T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261769.10:c.1587T>C MANE Select | ENSP00000261769.4:p.Thr529= | |
| ENST00000261769.9:c.1587T>C | ENSP00000261769.4:p.Thr529= | |
| ENST00000422392.6:c.1404T>C | ENSP00000414946.2:p.Thr468= | |
| ENST00000562836.5:n.1658T>C | ||
| ENST00000566510.5:c.*253T>C | ENSP00000458139.1:n.*253T>C | |
| ENST00000566612.5:c.1566-2700T>C | ENSP00000454782.1:n.1566-2700T>C | |
| ENST00000611625.4:c.1650T>C | ENSP00000481063.1:p.Thr550= | |
| ENST00000612417.4:c.1587T>C | ENSP00000478360.1:p.Thr529= | |
| ENST00000621016.4:c.1587T>C | ENSP00000480664.1:p.Thr529= | |
| NM_004360.3:c.1587T>C , LRG_301t1:c.1587T>C | NP_004351.1:p.Thr529= | |
| XM_011523488.1:c.852T>C | XP_011521790.1:p.Thr284= | |
| XM_011523489.1:c.852T>C | XP_011521791.1:p.Thr284= | |
| NM_001317184.1:c.1404T>C | NP_001304113.1:p.Thr468= | |
| NM_001317185.1:c.39T>C | NP_001304114.1:p.Thr13= | |
| NM_001317186.1:c.-254-2700T>C | NP_001304115.1:n.-254-2700T>C | |
| NM_004360.4:c.1587T>C | NP_004351.1:p.Thr529= | |
| NM_004360.5:c.1587T>C MANE Select | NP_004351.1:p.Thr529= | |
| NM_001317184.2:c.1404T>C | NP_001304113.1:p.Thr468= | |
| NM_001317185.2:c.39T>C | NP_001304114.1:p.Thr13= | |
| NM_001317186.2:c.-254-2700T>C | NP_001304115.1:n.-254-2700T>C |