Linked Data
gnomAD v4:
15-74339529-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74339529T>G , CM000677.2:g.74339529T>G | GRCh38 |
| NC_000015.9:g.74631870T>G , CM000677.1:g.74631870T>G | GRCh37 |
| NC_000015.8:g.72418923T>G | NCBI36 |
| NG_007973.1:g.33213A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268053.11:c.1157+58A>C MANE Select | ENSP00000268053.6:n.1157+58A>C | |
| ENST00000268053.10:c.1157+58A>C | ENSP00000268053.6:n.1157+58A>C | |
| ENST00000358632.8:c.683+58A>C | ENSP00000351455.4:n.683+58A>C | |
| ENST00000435365.5:c.1157+58A>C | ENSP00000391081.1:n.1157+58A>C | |
| NM_000781.2:c.1157+58A>C | NP_000772.2:n.1157+58A>C | |
| NM_001099773.1:c.683+58A>C | NP_001093243.1:n.683+58A>C | |
| NM_000781.3:c.1157+58A>C MANE Select | NP_000772.2:n.1157+58A>C | |
| NM_001099773.2:c.683+58A>C | NP_001093243.1:n.683+58A>C |