Linked Data
gnomAD v4:
1-11845942-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11845942A>G , CM000663.2:g.11845942A>G | GRCh38 |
| NC_000001.10:g.11905999A>G , CM000663.1:g.11905999A>G | GRCh37 |
| NC_000001.9:g.11828586A>G | NCBI36 |
| NG_012926.1:g.6842T>C , LRG_751:g.6842T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000400892.3:c.*1961+176A>G (CLCN6) | ENSP00000496938.1:n.*1961+176A>G | |
| ENST00000446542.5:n.781+176A>G (NPPA-AS1) | ||
| ENST00000376476.1:c.*67T>C (NPPA) | ENSP00000365659.1:n.*67T>C | |
| ENST00000376480.7:c.*67T>C (NPPA) MANE Select | ENSP00000365663.3:n.*67T>C | |
| ENST00000610706.1:c.*61T>C (NPPA) | ENSP00000483195.1:n.*61T>C | |
| NM_006172.3:c.*67T>C , LRG_751t1:c.*67T>C (NPPA) | NP_006163.1:n.*67T>C | |
| NR_037806.1:n.1479+176A>G (NPPA-AS1) | ||
| NM_006172.4:c.*67T>C (NPPA) MANE Select | NP_006163.1:n.*67T>C |