Linked Data
gnomAD v4:
19-12887154-CCA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887156_12887157del , CM000681.2:g.12887156_12887157del | GRCh38 |
| NC_000019.9:g.12997970_12997971del , CM000681.1:g.12997970_12997971del | GRCh37 |
| NC_000019.8:g.12858970_12858971del | NCBI36 |
| NG_009292.1:g.997_998del | |
| NG_013087.1:g.5048_5049del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.-16_-15del MANE Select | ENSP00000264834.3:n.-16_-15del | |
| ENST00000264834.4:c.-16_-15del | ENSP00000264834.3:n.-16_-15del | |
| NM_006563.3:c.-16_-15del | NP_006554.1:n.-16_-15del | |
| NM_006563.4:c.-16_-15del | NP_006554.1:n.-16_-15del | |
| NM_006563.5:c.-16_-15del MANE Select | NP_006554.1:n.-16_-15del |