Linked Data
gnomAD v4:
15-66703195-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66703195A>G , CM000677.2:g.66703195A>G | GRCh38 |
| NC_000015.9:g.66995533A>G , CM000677.1:g.66995533A>G | GRCh37 |
| NC_000015.8:g.64782587A>G | NCBI36 |
| NG_012244.1:g.5860A>G | |
| NG_012244.2:g.5860A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288840.10:c.-64A>G MANE Select | ENSP00000288840.5:n.-64A>G | |
| ENST00000288840.9:c.-64A>G | ENSP00000288840.5:n.-64A>G | |
| ENST00000612349.1:n.119A>G | ||
| NM_005585.4:c.-64A>G | NP_005576.3:n.-64A>G | |
| NR_027654.1:n.860A>G | ||
| XR_931825.1:n.1096A>G | ||
| XR_931826.1:n.1096A>G | ||
| XR_931827.1:n.1096A>G | ||
| XR_931827.2:n.1086A>G | ||
| NM_005585.5:c.-64A>G MANE Select | NP_005576.3:n.-64A>G | |
| NR_027654.2:n.960A>G |