Linked Data
ClinVar Variation Id:
285484
dbSNP Id:
rs530529988
ExAC:
15:42695039 C / T
gnomAD v2:
15-42695039-C-T
gnomAD v3:
15-42402841-C-T
gnomAD v4:
15-42402841-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42402841C>T , CM000677.2:g.42402841C>T | GRCh38 |
| NC_000015.9:g.42695039C>T , CM000677.1:g.42695039C>T | GRCh37 |
| NC_000015.8:g.40482331C>T | NCBI36 |
| NG_008660.1:g.59739C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1440C>T | ENSP00000183936.4:p.Asn480= | |
| ENST00000357568.8:c.1584C>T | ENSP00000350181.3:p.Asn528= | |
| ENST00000397163.8:c.1584C>T MANE Select | ENSP00000380349.3:p.Asn528= | |
| ENST00000466369.5:n.2093C>T | ||
| ENST00000483208.5:n.2473C>T | ||
| ENST00000495723.1:n.2473C>T | ||
| ENST00000549793.5:n.1815C>T | ||
| ENST00000638141.2:n.1455C>T | ||
| ENST00000673646.1:c.48C>T | ENSP00000501007.1:p.Asn16= | |
| ENST00000673705.1:c.309+3189C>T | ENSP00000501021.1:n.309+3189C>T | |
| ENST00000673813.1:n.506C>T | ||
| ENST00000318023.11:c.1440C>T | ENSP00000326281.8:p.Asn480= | |
| ENST00000349748.7:c.1440C>T | ENSP00000183936.4:p.Asn480= | |
| ENST00000357568.7:c.1584C>T | ENSP00000350181.3:p.Asn528= | |
| ENST00000397163.7:c.1584C>T | ENSP00000380349.3:p.Asn528= | |
| ENST00000397200.8:c.48C>T | ENSP00000380384.4:p.Asn16= | |
| ENST00000567071.5:c.43C>T | ||
| ENST00000569827.5:c.48C>T | ENSP00000454379.1:p.Asn16= | |
| NM_000070.2:c.1584C>T | NP_000061.1:p.Asn528= | |
| NM_024344.1:c.1584C>T | NP_077320.1:p.Asn528= | |
| NM_173087.1:c.1440C>T | NP_775110.1:p.Asn480= | |
| NM_173088.1:c.48C>T | NP_775111.1:p.Asn16= | |
| NM_000070.3:c.1584C>T MANE Select | NP_000061.1:p.Asn528= | |
| NM_024344.2:c.1584C>T | NP_077320.1:p.Asn528= | |
| NM_173087.2:c.1440C>T | NP_775110.1:p.Asn480= | |
| NM_173088.2:c.48C>T | NP_775111.1:p.Asn16= |