Linked Data
gnomAD v4:
1-11845862-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11845862G>T , CM000663.2:g.11845862G>T | GRCh38 |
| NC_000001.10:g.11905919G>T , CM000663.1:g.11905919G>T | GRCh37 |
| NC_000001.9:g.11828506G>T | NCBI36 |
| NG_012926.1:g.6922C>A , LRG_751:g.6922C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1961+96G>T (CLCN6) | ENSP00000496938.1:n.*1961+96G>T | |
| ENST00000446542.5:n.781+96G>T (NPPA-AS1) | ||
| ENST00000376480.7:c.*147C>A (NPPA) MANE Select | ENSP00000365663.3:n.*147C>A | |
| ENST00000610706.1:c.*141C>A (NPPA) | ENSP00000483195.1:n.*141C>A | |
| NM_006172.3:c.*147C>A , LRG_751t1:c.*147C>A (NPPA) | NP_006163.1:n.*147C>A | |
| NR_037806.1:n.1479+96G>T (NPPA-AS1) | ||
| NM_006172.4:c.*147C>A (NPPA) MANE Select | NP_006163.1:n.*147C>A |