Linked Data
gnomAD v4:
8-95247609-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.95247609C>T , CM000670.2:g.95247609C>T | GRCh38 |
| NC_000008.10:g.96259837C>T , CM000670.1:g.96259837C>T | GRCh37 |
| NC_000008.9:g.96329013C>T | NCBI36 |
| NG_032804.1:g.26626G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286688.6:c.*8G>A MANE Select | ENSP00000286688.5:n.*8G>A | |
| ENST00000286688.5:c.*8G>A | ENSP00000286688.5:n.*8G>A | |
| NM_177965.3:c.*8G>A | NP_808880.1:n.*8G>A | |
| XM_005250799.2:c.*8G>A | XP_005250856.2:n.*8G>A | |
| NM_001363260.1:c.*8G>A | NP_001350189.1:n.*8G>A | |
| NM_177965.4:c.*8G>A MANE Select | NP_808880.1:n.*8G>A |