Linked Data
gnomAD v4:
1-34781661-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34781661C>T , CM000663.2:g.34781661C>T | GRCh38 |
| NC_000001.10:g.35247262C>T , CM000663.1:g.35247262C>T | GRCh37 |
| NC_000001.9:g.35019849C>T | NCBI36 |
| NG_008309.1:g.5473C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373366.3:c.-143C>T (GJB3) MANE Select | ENSP00000362464.2:n.-143C>T | |
| ENST00000373366.2:c.-143C>T (GJB3) | ENSP00000362464.2:n.-143C>T | |
| ENST00000426886.1:c.208-63252G>A (SMIM12) | ENSP00000429902.1:n.208-63252G>A | |
| NM_024009.2:c.-143C>T (GJB3) | NP_076872.1:n.-143C>T | |
| XR_947179.1:n.1001+16710G>A | ||
| XR_001737967.1:n.1023+16710G>A | ||
| NM_024009.3:c.-143C>T (GJB3) MANE Select | NP_076872.1:n.-143C>T |