Linked Data
gnomAD v4:
1-11845876-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11845876C>A , CM000663.2:g.11845876C>A | GRCh38 |
| NC_000001.10:g.11905933C>A , CM000663.1:g.11905933C>A | GRCh37 |
| NC_000001.9:g.11828520C>A | NCBI36 |
| NG_012926.1:g.6908G>T , LRG_751:g.6908G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1961+110C>A (CLCN6) | ENSP00000496938.1:n.*1961+110C>A | |
| ENST00000446542.5:n.781+110C>A (NPPA-AS1) | ||
| ENST00000376480.7:c.*133G>T (NPPA) MANE Select | ENSP00000365663.3:n.*133G>T | |
| ENST00000610706.1:c.*127G>T (NPPA) | ENSP00000483195.1:n.*127G>T | |
| NM_006172.3:c.*133G>T , LRG_751t1:c.*133G>T (NPPA) | NP_006163.1:n.*133G>T | |
| NR_037806.1:n.1479+110C>A (NPPA-AS1) | ||
| NM_006172.4:c.*133G>T (NPPA) MANE Select | NP_006163.1:n.*133G>T |