Linked Data
gnomAD v4:
19-1106785-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1106787dup , CM000681.2:g.1106787dup | GRCh38 |
| NC_000019.9:g.1106786dup , CM000681.1:g.1106786dup | GRCh37 |
| NC_000019.8:g.1057786dup | NCBI36 |
| NG_050621.1:g.7862dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354171.12:c.*215dup | ENSP00000346103.7:n.*215dup | |
| ENST00000588919.5:c.*21dup | ENSP00000464989.3:n.*21dup | |
| ENST00000592940.2:n.1180dup | ||
| NM_001039847.2:c.*147dup | NP_001034936.1:n.*147dup | |
| NM_001039848.2:c.*215dup | NP_001034937.1:n.*215dup | |
| NM_002085.4:c.*215dup | NP_002076.2:n.*215dup | |
| NM_001039848.3:c.*215dup | NP_001034937.1:n.*215dup |