Linked Data
gnomAD v4:
15-73368123-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73368123G>C , CM000677.2:g.73368123G>C | GRCh38 |
| NC_000015.9:g.73660464G>C , CM000677.1:g.73660464G>C | GRCh37 |
| NC_000015.8:g.71447517G>C | NCBI36 |
| NG_009063.1:g.6142C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.148C>G MANE Select | ENSP00000261917.3:p.Leu50Val | |
| ENST00000261917.3:c.148C>G | ENSP00000261917.3:p.Leu50Val | |
| NM_005477.2:c.148C>G | NP_005468.1:p.Leu50Val | |
| NM_005477.3:c.148C>G MANE Select | NP_005468.1:p.Leu50Val |