Linked Data
dbSNP Id:
rs1048046426
gnomAD v4:
1-34781739-G-A
MyVariant Identifiers:
chr1:g.34781739G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34781739G>A , CM000663.2:g.34781739G>A | GRCh38 |
| NC_000001.10:g.35247340G>A , CM000663.1:g.35247340G>A | GRCh37 |
| NC_000001.9:g.35019927G>A | NCBI36 |
| NG_008309.1:g.5551G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373366.3:c.-65G>A (GJB3) MANE Select | ENSP00000362464.2:n.-65G>A | |
| ENST00000373366.2:c.-65G>A (GJB3) | ENSP00000362464.2:n.-65G>A | |
| ENST00000426886.1:c.208-63330C>T (SMIM12) | ENSP00000429902.1:n.208-63330C>T | |
| NM_024009.2:c.-65G>A (GJB3) | NP_076872.1:n.-65G>A | |
| XR_947179.1:n.1001+16632C>T | ||
| XR_001737967.1:n.1023+16632C>T | ||
| NM_024009.3:c.-65G>A (GJB3) MANE Select | NP_076872.1:n.-65G>A |