Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49954233G>T , CM000674.2:g.49954233G>T | GRCh38 |
| NC_000012.11:g.50348016G>T , CM000674.1:g.50348016G>T | GRCh37 |
| NC_000012.10:g.48634283G>T | NCBI36 |
| NG_008913.1:g.8493G>T , LRG_717:g.8493G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000486.6:c.439G>T (AQP2) MANE Select | NP_000477.1:p.Ala147Ser |
| ENST00000199280.4:c.439G>T (AQP2) MANE Select | ENSP00000199280.3:p.Ala147Ser |
| NM_000486.5:c.439G>T , LRG_717t1:c.439G>T (AQP2) | NP_000477.1:p.Ala147Ser |
| NR_110590.1:n.372C>A (AQP5-AS1) | |
| NR_110591.1:n.118-2145C>A (AQP5-AS1) | |
| ENST00000199280.3:c.439G>T (AQP2) | ENSP00000199280.3:p.Ala147Ser |
| ENST00000550862.1:c.439G>T (AQP2) | ENSP00000450022.1:p.Ala147Ser |
| ENST00000551526.5:c.439G>T (AQP2) | ENSP00000447148.1:p.Ala147Ser |