Linked Data
gnomAD v4:
15-40472475-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40472475C>T , CM000677.2:g.40472475C>T | GRCh38 |
| NC_000015.9:g.40764674C>T , CM000677.1:g.40764674C>T | GRCh37 |
| NC_000015.8:g.38551966C>T | NCBI36 |
| NG_017074.1:g.6515C>T , LRG_600:g.6515C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.*131C>T MANE Select | ENSP00000307297.6:n.*131C>T | |
| ENST00000306243.6:c.*131C>T | ENSP00000307297.5:n.*131C>T | |
| ENST00000559991.1:c.*131C>T | ENSP00000453882.1:n.*131C>T | |
| NM_130468.3:c.*131C>T , LRG_600t1:c.*131C>T | NP_569735.1:n.*131C>T | |
| NM_130468.4:c.*131C>T MANE Select | NP_569735.1:n.*131C>T |