Linked Data
ClinVar Variation Id:
1103371
dbSNP Id:
rs111972793
ExAC:
15:80454631 C / T
gnomAD v2:
15-80454631-C-T
gnomAD v3:
15-80162289-C-T
gnomAD v4:
15-80162289-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80162289C>T , CM000677.2:g.80162289C>T | GRCh38 |
| NC_000015.9:g.80454631C>T , CM000677.1:g.80454631C>T | GRCh37 |
| NC_000015.8:g.78241686C>T | NCBI36 |
| NG_012833.1:g.14291C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558767.6:c.408C>T | ENSP00000507680.1:p.Asn136= | |
| ENST00000682012.1:n.483C>T | ||
| ENST00000683593.1:n.2071C>T | ||
| ENST00000684363.1:c.365-103C>T | ENSP00000507314.1:n.365-103C>T | |
| ENST00000684569.1:n.453C>T | ||
| ENST00000561421.6:c.408C>T MANE Select | ENSP00000453347.2:p.Asn136= | |
| ENST00000646551.1:n.1895C>T | ||
| ENST00000261755.9:c.408C>T | ENSP00000261755.5:p.Asn136= | |
| ENST00000407106.5:c.408C>T | ENSP00000385080.1:p.Asn136= | |
| ENST00000537726.5:n.554C>T | ||
| ENST00000539156.5:c.198C>T | ENSP00000454271.1:p.Asn66= | |
| ENST00000558022.5:c.408C>T | ENSP00000453152.1:p.Asn136= | |
| ENST00000558627.1:n.336C>T | ||
| ENST00000558767.5:n.669C>T | ||
| ENST00000561369.1:n.552C>T | ||
| ENST00000561421.5:c.408C>T | ENSP00000453347.1:p.Asn136= | |
| NM_000137.2:c.408C>T | NP_000128.1:p.Asn136= | |
| XM_024449872.1:c.408C>T | XP_024305640.1:p.Asn136= | |
| NM_000137.4:c.408C>T MANE Select | NP_000128.1:p.Asn136= | |
| NM_001374377.1:c.408C>T | NP_001361306.1:p.Asn136= | |
| NM_001374380.1:c.408C>T | NP_001361309.1:p.Asn136= |