Linked Data
ClinVar Variation Id:
462791
dbSNP Id:
rs144841836
ExAC:
1:161279672 G / A
gnomAD v2:
1-161279672-G-A
gnomAD v3:
1-161309882-G-A
gnomAD v4:
1-161309882-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161309882G>A , CM000663.2:g.161309882G>A | GRCh38 |
| NC_000001.10:g.161279672G>A , CM000663.1:g.161279672G>A | GRCh37 |
| NC_000001.9:g.159546296G>A | NCBI36 |
| NG_008055.1:g.5091C>T , LRG_256:g.5091C>T | |
| NG_012767.1:g.507G>A , LRG_317:g.507G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526189.3:c.24C>T | ENSP00000488104.2:p.Ser8= | |
| ENST00000533357.5:c.24C>T MANE Select | ENSP00000432943.1:p.Ser8= | |
| ENST00000672602.2:c.24C>T | ENSP00000500814.2:p.Ser8= | |
| ENST00000674861.1:n.87C>T | ||
| ENST00000463290.5:c.24C>T | ENSP00000431538.1:p.Ser8= | |
| ENST00000533357.4:c.24C>T | ENSP00000432943.1:p.Ser8= | |
| NM_000530.6:c.24C>T , LRG_256t1:c.24C>T | NP_000521.2:p.Ser8= | |
| NM_000530.7:c.24C>T | NP_000521.2:p.Ser8= | |
| NM_001315491.1:c.24C>T | NP_001302420.1:p.Ser8= | |
| XM_017001321.2:c.54C>T | XP_016856810.1:p.Ser18= | |
| NM_000530.8:c.24C>T MANE Select | NP_000521.2:p.Ser8= | |
| NM_001315491.2:c.24C>T | NP_001302420.1:p.Ser8= |