Revel Score:
ENST00000373366 (MANE Select)
0.364
ENST00000373362
0.364
ENST00000543647
0.364
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34785259A>T , CM000663.2:g.34785259A>T | GRCh38 |
| NC_000001.10:g.35250860A>T , CM000663.1:g.35250860A>T | GRCh37 |
| NC_000001.9:g.35023447A>T | NCBI36 |
| NG_008309.1:g.9071A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373366.3:c.497A>T (GJB3) MANE Select | ENSP00000362464.2:p.Asn166Ile | |
| ENST00000373362.3:c.497A>T (GJB3) | ENSP00000362460.3:p.Asn166Ile | |
| ENST00000373366.2:c.497A>T (GJB3) | ENSP00000362464.2:p.Asn166Ile | |
| ENST00000426886.1:c.208-66850T>A (SMIM12) | ENSP00000429902.1:n.208-66850T>A | |
| NM_001005752.1:c.497A>T (GJB3) | NP_001005752.1:p.Asn166Ile | |
| NM_024009.2:c.497A>T (GJB3) | NP_076872.1:p.Asn166Ile | |
| XR_947179.1:n.1001+13112T>A | ||
| XR_001737967.1:n.1023+13112T>A | ||
| NM_024009.3:c.497A>T (GJB3) MANE Select | NP_076872.1:p.Asn166Ile | |
| NM_001005752.2:c.497A>T (GJB3) | NP_001005752.1:p.Asn166Ile |