Linked Data
dbSNP Id:
rs765425113
ExAC:
16:4847898 T / A
gnomAD v2:
16-4847898-T-A
gnomAD v3:
16-4797897-T-A
gnomAD v4:
16-4797897-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.4797897T>A , CM000678.2:g.4797897T>A | GRCh38 |
| NC_000016.9:g.4847898T>A , CM000678.1:g.4847898T>A | GRCh37 |
| NC_000016.8:g.4787899T>A | NCBI36 |
| NG_032174.1:g.10054A>T , LRG_455:g.10054A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322048.12:c.695+41A>T MANE Select | ENSP00000322832.6:n.695+41A>T | |
| ENST00000322048.11:c.695+41A>T | ENSP00000322832.5:n.695+41A>T | |
| ENST00000586153.1:c.341+41A>T | ENSP00000464699.1:n.341+41A>T | |
| ENST00000586336.5:n.794+41A>T | ||
| ENST00000586504.5:c.426-57A>T | ||
| ENST00000587377.5:c.*15+41A>T | ENSP00000468343.1:n.*15+41A>T | |
| ENST00000587711.5:c.380+41A>T | ENSP00000467459.1:n.380+41A>T | |
| ENST00000587843.5:c.*433+41A>T | ENSP00000465970.1:n.*433+41A>T | |
| ENST00000588201.5:c.*686+41A>T | ENSP00000466529.1:n.*686+41A>T | |
| ENST00000589543.5:n.652+41A>T | ||
| ENST00000591292.5:n.2024+41A>T | ||
| ENST00000591392.5:c.623+41A>T | ENSP00000467509.1:n.623+41A>T | |
| ENST00000592019.1:c.77-82A>T | ||
| NM_024589.2:c.695+41A>T , LRG_455t1:c.695+41A>T | NP_078865.1:n.695+41A>T | |
| NR_046480.1:n.1019+41A>T | ||
| XM_006720947.2:c.696-36A>T | XP_006721010.1:n.696-36A>T | |
| XM_006720948.2:c.426-36A>T | XP_006721011.1:n.426-36A>T | |
| XM_006720947.4:c.696-36A>T | XP_006721010.1:n.696-36A>T | |
| XM_006720948.4:c.426-36A>T | XP_006721011.1:n.426-36A>T | |
| NM_024589.3:c.695+41A>T MANE Select | NP_078865.1:n.695+41A>T | |
| NR_046480.2:n.702+41A>T |