Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216073275A>G , CM000663.2:g.216073275A>G | GRCh38 |
| NC_000001.10:g.216246617A>G , CM000663.1:g.216246617A>G | GRCh37 |
| NC_000001.9:g.214313240A>G | NCBI36 |
| NG_009497.1:g.355122T>C | |
| NG_009497.2:g.355174T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_206933.4:c.5598T>C (USH2A) MANE Select | NP_996816.3:p.Val1866= |
| ENST00000307340.8:c.5598T>C (USH2A) MANE Select | ENSP00000305941.3:p.Val1866= |
| NM_206933.2:c.5598T>C (USH2A) | NP_996816.2:p.Val1866= |
| NM_206933.3:c.5598T>C (USH2A) | NP_996816.2:p.Val1866= |
| NR_125992.1:n.136+675A>G (USH2A-AS2) | |
| NR_125993.1:n.136+675A>G (USH2A-AS2) | |
| ENST00000307340.7:c.5598T>C (USH2A) | ENSP00000305941.3:p.Val1866= |
| ENST00000674083.1:c.5598T>C (USH2A) | ENSP00000501296.1:p.Val1866= |