Linked Data
gnomAD v4:
17-47733480-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47733480G>T , CM000679.2:g.47733480G>T | GRCh38 |
| NC_000017.10:g.45810846G>T , CM000679.1:g.45810846G>T | GRCh37 |
| NC_000017.9:g.43165845G>T | NCBI36 |
| NG_012166.1:g.5237G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.26G>T MANE Select | ENSP00000177694.1:p.Gly9Val | |
| ENST00000177694.1:c.26G>T | ENSP00000177694.1:p.Gly9Val | |
| ENST00000581328.1:n.56G>T | ||
| NM_013351.1:c.26G>T | NP_037483.1:p.Gly9Val | |
| XM_011524698.1:c.26G>T | XP_011523000.1:p.Gly9Val | |
| NM_013351.2:c.26G>T MANE Select | NP_037483.1:p.Gly9Val |