Linked Data
gnomAD v4:
19-6713652-G-GGC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713652_6713653insGC , CM000681.2:g.6713652_6713653insGC | GRCh38 |
| NC_000019.9:g.6713663_6713664insGC , CM000681.1:g.6713663_6713664insGC | GRCh37 |
| NC_000019.8:g.6664663_6664664insGC | NCBI36 |
| NG_009557.1:g.11999_12000insGC , LRG_27:g.11999_12000insGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.651-144_651-143insGC | ENSP00000512083.1:n.651-144_651-143insGC | |
| ENST00000245907.11:c.774-144_774-143insGC MANE Select | ENSP00000245907.4:n.774-144_774-143insGC | |
| ENST00000245907.10:c.774-144_774-143insGC | ENSP00000245907.4:n.774-144_774-143insGC | |
| ENST00000595577.1:n.278-144_278-143insGC | ||
| ENST00000597442.5:n.23+113_23+114insGC | ||
| NM_000064.3:c.774-144_774-143insGC | NP_000055.2:n.774-144_774-143insGC | |
| NM_000064.4:c.774-144_774-143insGC MANE Select | NP_000055.2:n.774-144_774-143insGC |