Linked Data
gnomAD v4:
1-34781523-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34781523T>C , CM000663.2:g.34781523T>C | GRCh38 |
| NC_000001.10:g.35247124T>C , CM000663.1:g.35247124T>C | GRCh37 |
| NC_000001.9:g.35019711T>C | NCBI36 |
| NG_008309.1:g.5335T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373366.3:c.-281T>C (GJB3) MANE Select | ENSP00000362464.2:n.-281T>C | |
| ENST00000373366.2:c.-281T>C (GJB3) | ENSP00000362464.2:n.-281T>C | |
| ENST00000426886.1:c.208-63114A>G (SMIM12) | ENSP00000429902.1:n.208-63114A>G | |
| NM_024009.2:c.-281T>C (GJB3) | NP_076872.1:n.-281T>C | |
| XR_947179.1:n.1001+16848A>G | ||
| XR_001737967.1:n.1023+16848A>G | ||
| NM_024009.3:c.-281T>C (GJB3) MANE Select | NP_076872.1:n.-281T>C |