Linked Data
ClinVar Variation Id:
1949976
ClinVar RCV Id:
RCV002671356
dbSNP Id:
rs752897835
ExAC:
15:80445417 C / T
gnomAD v2:
15-80445417-C-T
gnomAD v4:
15-80153075-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80153075C>T , CM000677.2:g.80153075C>T | GRCh38 |
| NC_000015.9:g.80445417C>T , CM000677.1:g.80445417C>T | GRCh37 |
| NC_000015.8:g.78232472C>T | NCBI36 |
| NG_012833.1:g.5077C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000558767.6:c.21C>T | ENSP00000507680.1:p.Ala7= | |
| ENST00000682012.1:n.96C>T | ||
| ENST00000684363.1:c.21C>T | ENSP00000507314.1:p.Ala7= | |
| ENST00000684569.1:n.66C>T | ||
| ENST00000561421.6:c.21C>T MANE Select | ENSP00000453347.2:p.Ala7= | |
| ENST00000261755.9:c.21C>T | ENSP00000261755.5:p.Ala7= | |
| ENST00000407106.5:c.21C>T | ENSP00000385080.1:p.Ala7= | |
| ENST00000537726.5:n.103C>T | ||
| ENST00000558022.5:c.21C>T | ENSP00000453152.1:p.Ala7= | |
| ENST00000558767.5:n.282C>T | ||
| ENST00000561369.1:n.101C>T | ||
| ENST00000561421.5:c.21C>T | ENSP00000453347.1:p.Ala7= | |
| NM_000137.2:c.21C>T | NP_000128.1:p.Ala7= | |
| XM_024449872.1:c.21C>T | XP_024305640.1:p.Ala7= | |
| NM_000137.4:c.21C>T MANE Select | NP_000128.1:p.Ala7= | |
| NM_001374377.1:c.21C>T | NP_001361306.1:p.Ala7= | |
| NM_001374380.1:c.21C>T | NP_001361309.1:p.Ala7= |