Linked Data
gnomAD v4:
17-1650651-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.1650651A>T , CM000679.2:g.1650651A>T | GRCh38 |
| NC_000017.10:g.1553945A>T , CM000679.1:g.1553945A>T | GRCh37 |
| NC_000017.9:g.1500695A>T | NCBI36 |
| NG_009118.1:g.39232T>A | |
| NG_033061.1:g.4448T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304992.11:c.*151T>A MANE Select | ENSP00000304350.6:n.*151T>A | |
| ENST00000304992.10:c.*151T>A | ENSP00000304350.6:n.*151T>A | |
| ENST00000571958.1:c.358T>A | ||
| ENST00000572621.5:c.*151T>A | ENSP00000460348.1:n.*151T>A | |
| NM_006445.3:c.*151T>A | NP_006436.3:n.*151T>A | |
| XM_024450537.1:c.*151T>A | XP_024306305.1:n.*151T>A | |
| NM_006445.4:c.*151T>A MANE Select | NP_006436.3:n.*151T>A |