Linked Data
gnomAD v4:
15-73367892-CCG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367895_73367896del , CM000677.2:g.73367895_73367896del | GRCh38 |
| NC_000015.9:g.73660236_73660237del , CM000677.1:g.73660236_73660237del | GRCh37 |
| NC_000015.8:g.71447289_71447290del | NCBI36 |
| NG_009063.1:g.6371_6372del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.377_378del MANE Select | ENSP00000261917.3:p.Ala126GlyfsTer? | |
| ENST00000261917.3:c.377_378del | ENSP00000261917.3:p.Ala126GlyfsTer? | |
| NM_005477.2:c.377_378del | NP_005468.1:p.Ala126GlyfsTer? | |
| NM_005477.3:c.377_378del MANE Select | NP_005468.1:p.Ala126GlyfsTer? |