Linked Data
gnomAD v4:
1-34781642-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34781642T>C , CM000663.2:g.34781642T>C | GRCh38 |
| NC_000001.10:g.35247243T>C , CM000663.1:g.35247243T>C | GRCh37 |
| NC_000001.9:g.35019830T>C | NCBI36 |
| NG_008309.1:g.5454T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373366.3:c.-162T>C (GJB3) MANE Select | ENSP00000362464.2:n.-162T>C | |
| ENST00000373366.2:c.-162T>C (GJB3) | ENSP00000362464.2:n.-162T>C | |
| ENST00000426886.1:c.208-63233A>G (SMIM12) | ENSP00000429902.1:n.208-63233A>G | |
| NM_024009.2:c.-162T>C (GJB3) | NP_076872.1:n.-162T>C | |
| XR_947179.1:n.1001+16729A>G | ||
| XR_001737967.1:n.1023+16729A>G | ||
| NM_024009.3:c.-162T>C (GJB3) MANE Select | NP_076872.1:n.-162T>C |