Linked Data
gnomAD v4:
15-40472352-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40472352T>C , CM000677.2:g.40472352T>C | GRCh38 |
| NC_000015.9:g.40764551T>C , CM000677.1:g.40764551T>C | GRCh37 |
| NC_000015.8:g.38551843T>C | NCBI36 |
| NG_017074.1:g.6392T>C , LRG_600:g.6392T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.*8T>C MANE Select | ENSP00000307297.6:n.*8T>C | |
| ENST00000306243.6:c.*8T>C | ENSP00000307297.5:n.*8T>C | |
| ENST00000559991.1:c.*8T>C | ENSP00000453882.1:n.*8T>C | |
| NM_130468.3:c.*8T>C , LRG_600t1:c.*8T>C | NP_569735.1:n.*8T>C | |
| NM_130468.4:c.*8T>C MANE Select | NP_569735.1:n.*8T>C |