Linked Data
ClinVar Variation Id:
2900035
ClinVar RCV Id:
RCV003632637
dbSNP Id:
rs1246253610
gnomAD v4:
1-11846032-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11846032A>T , CM000663.2:g.11846032A>T | GRCh38 |
| NC_000001.10:g.11906089A>T , CM000663.1:g.11906089A>T | GRCh37 |
| NC_000001.9:g.11828676A>T | NCBI36 |
| NG_012926.1:g.6752T>A , LRG_751:g.6752T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1961+266A>T (CLCN6) | ENSP00000496938.1:n.*1961+266A>T | |
| ENST00000446542.5:n.781+266A>T (NPPA-AS1) | ||
| ENST00000376476.1:c.301-18T>A (NPPA) | ENSP00000365659.1:n.301-18T>A | |
| ENST00000376480.7:c.451-18T>A (NPPA) MANE Select | ENSP00000365663.3:n.451-18T>A | |
| ENST00000610706.1:c.451-18T>A (NPPA) | ENSP00000483195.1:n.451-18T>A | |
| NM_006172.3:c.451-18T>A , LRG_751t1:c.451-18T>A (NPPA) | NP_006163.1:n.451-18T>A | |
| NR_037806.1:n.1479+266A>T (NPPA-AS1) | ||
| NM_006172.4:c.451-18T>A (NPPA) MANE Select | NP_006163.1:n.451-18T>A |