Linked Data
gnomAD v4:
15-40405750-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40405750T>G , CM000677.2:g.40405750T>G | GRCh38 |
| NC_000015.9:g.40697951T>G , CM000677.1:g.40697951T>G | GRCh37 |
| NC_000015.8:g.38485243T>G | NCBI36 |
| NG_011986.1:g.5266T>G | |
| NG_011986.2:g.5266T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650656.1:c.-69T>G | ENSP00000498731.1:n.-69T>G | |
| ENST00000651168.1:c.-69T>G | ENSP00000499074.1:n.-69T>G | |
| NM_001159508.1:c.-69T>G | NP_001152980.1:n.-69T>G | |
| NM_002225.3:c.-69T>G | NP_002216.2:n.-69T>G | |
| XR_429453.2:n.33T>G |