Linked Data
gnomAD v4:
19-45766579-C-CG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45766584dup , CM000681.2:g.45766584dup | GRCh38 |
| NC_000019.9:g.46269842dup , CM000681.1:g.46269842dup | GRCh37 |
| NC_000019.8:g.50961682dup | NCBI36 |
| NG_012745.1:g.7660dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317578.7:c.1379dup MANE Select | ENSP00000316842.4:p.Tyr462ValfsTer? | |
| ENST00000317578.6:c.1379dup | ENSP00000316842.4:p.Tyr462ValfsTer? | |
| ENST00000560160.1:c.587-469dup | ||
| ENST00000560168.1:c.*567dup | ENSP00000453189.2:n.*567dup | |
| ENST00000622857.1:c.16-618dup | ENSP00000481365.1:n.16-618dup | |
| NM_175875.4:c.1379dup | NP_787071.2:p.Tyr462ValfsTer? | |
| NM_175875.5:c.1379dup MANE Select | NP_787071.3:p.Tyr462ValfsTer? |