Linked Data
ClinVar Variation Id:
1048486
ClinVar RCV Id:
RCV001578591
dbSNP Id:
rs368305568
gnomAD v4:
16-88826798-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88826798G>T , CM000678.2:g.88826798G>T | GRCh38 |
| NC_000016.9:g.88893206G>T , CM000678.1:g.88893206G>T | GRCh37 |
| NC_000016.8:g.87420707G>T | NCBI36 |
| NG_008667.1:g.35169C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.1043C>A MANE Select | ENSP00000268695.5:p.Thr348Asn | |
| ENST00000268695.9:c.1043C>A | ENSP00000268695.5:p.Thr348Asn | |
| ENST00000562593.5:n.4452C>A | ||
| ENST00000564263.1:n.319C>A | ||
| ENST00000567525.5:c.724C>A | ENSP00000454484.1:n.724C>A | |
| ENST00000568613.5:c.1162C>A | ENSP00000457921.1:n.1162C>A | |
| NM_000512.4:c.1043C>A | NP_000503.1:p.Thr348Asn | |
| XM_005256301.2:c.1043C>A | XP_005256358.1:p.Thr348Asn | |
| XM_005256302.1:c.1061C>A | XP_005256359.1:p.Thr354Asn | |
| XM_011522982.1:c.1061C>A | XP_011521284.1:p.Thr354Asn | |
| XM_011522984.1:c.1061C>A | XP_011521286.1:p.Thr354Asn | |
| NM_001323543.1:c.488C>A | NP_001310472.1:p.Thr163Asn | |
| NM_001323544.1:c.1061C>A | NP_001310473.1:p.Thr354Asn | |
| XM_005256301.3:c.1043C>A | XP_005256358.1:p.Thr348Asn | |
| XM_011522982.2:c.1061C>A | XP_011521284.1:p.Thr354Asn | |
| XM_017023111.2:c.1061C>A | XP_016878600.1:p.Thr354Asn | |
| XM_017023112.2:c.1061C>A | XP_016878601.1:p.Thr354Asn | |
| XM_017023113.1:c.488C>A | XP_016878602.1:p.Thr163Asn | |
| NM_000512.5:c.1043C>A MANE Select | NP_000503.1:p.Thr348Asn | |
| NM_001323543.2:c.488C>A | NP_001310472.1:p.Thr163Asn | |
| NM_001323544.2:c.1061C>A | NP_001310473.1:p.Thr354Asn |