Linked Data
ClinVar Variation Id:
1350220
ClinVar RCV Id:
RCV002039589
dbSNP Id:
rs1801164691
gnomAD v4:
8-28716964-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.28716964C>A , CM000670.2:g.28716964C>A | GRCh38 |
| NC_000008.10:g.28574481C>A , CM000670.1:g.28574481C>A | GRCh37 |
| NC_000008.9:g.28630400C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696177.1:c.905C>A | ENSP00000512467.1:p.Thr302Asn | |
| ENST00000696178.1:c.905C>A | ENSP00000512468.1:p.Thr302Asn | |
| ENST00000696179.1:c.905C>A | ENSP00000512469.1:p.Thr302Asn | |
| ENST00000696180.1:c.905C>A | ENSP00000512470.1:p.Thr302Asn | |
| ENST00000696181.1:c.905C>A | ENSP00000512471.1:p.Thr302Asn | |
| ENST00000696182.1:c.-114-14259C>A | ENSP00000512472.1:n.-114-14259C>A | |
| ENST00000696184.1:c.905C>A | ENSP00000512473.1:p.Thr302Asn | |
| ENST00000696185.1:n.1538C>A | ||
| ENST00000696186.1:c.905C>A | ENSP00000512474.1:p.Thr302Asn | |
| ENST00000220562.9:c.905C>A MANE Select | ENSP00000220562.4:p.Thr302Asn | |
| ENST00000220562.8:c.905C>A | ENSP00000220562.4:p.Thr302Asn | |
| ENST00000519886.5:n.631+898C>A | ||
| ENST00000521532.5:c.42+6461C>A | ENSP00000431013.1:n.42+6461C>A | |
| ENST00000522698.1:c.213+67C>A | ||
| ENST00000523149.5:c.28-275C>A | ENSP00000428691.1:n.28-275C>A | |
| NM_001440.3:c.905C>A | NP_001431.1:p.Thr302Asn | |
| NR_073468.1:n.188-14259C>A | ||
| NR_073469.1:n.763+898C>A | ||
| XM_011544440.1:c.905C>A | XP_011542742.1:p.Thr302Asn | |
| XM_011544440.3:c.905C>A | XP_011542742.1:p.Thr302Asn | |
| XM_024447094.1:c.905C>A | XP_024302862.1:p.Thr302Asn | |
| XM_024447095.1:c.905C>A | XP_024302863.1:p.Thr302Asn | |
| XM_024447096.1:c.905C>A | XP_024302864.1:p.Thr302Asn | |
| NM_001440.4:c.905C>A MANE Select | NP_001431.1:p.Thr302Asn | |
| NR_073468.2:n.160-14259C>A | ||
| NR_073469.2:n.735+898C>A |