Linked Data
ClinVar Variation Id:
793642
ClinVar RCV Id:
RCV000976833
dbSNP Id:
rs756866064
ExAC:
16:81399057 C / T
gnomAD v2:
16-81399057-C-T
gnomAD v4:
16-81365452-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81365452C>T , CM000678.2:g.81365452C>T | GRCh38 |
| NC_000016.9:g.81399057C>T , CM000678.1:g.81399057C>T | GRCh37 |
| NC_000016.8:g.79956558C>T | NCBI36 |
| NG_009007.1:g.55487C>T , LRG_242:g.55487C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*1184C>T | ENSP00000498114.1:n.*1184C>T | |
| ENST00000648994.2:c.1476C>T MANE Select | ENSP00000497351.1:p.Ser492= | |
| ENST00000650388.1:c.1010C>T | ENSP00000498081.1:n.1010C>T | |
| ENST00000567335.1:n.34C>T | ||
| ENST00000568107.2:c.1476C>T | ENSP00000476795.1:p.Ser492= | |
| NM_022041.3:c.1476C>T , LRG_242t1:c.1476C>T | NP_071324.1:p.Ser492= | |
| XM_017023734.1:c.837C>T | XP_016879223.1:p.Ser279= | |
| NM_001377486.1:c.837C>T | NP_001364415.1:p.Ser279= | |
| NM_022041.4:c.1476C>T MANE Select | NP_071324.1:p.Ser492= |