Linked Data
gnomAD v4:
19-12887183-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887183_12887184insA , CM000681.2:g.12887183_12887184insA | GRCh38 |
| NC_000019.9:g.12997997_12997998insA , CM000681.1:g.12997997_12997998insA | GRCh37 |
| NC_000019.8:g.12858997_12858998insA | NCBI36 |
| NG_009292.1:g.1024_1025insA | |
| NG_013087.1:g.5020_5021insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.-44_-43insT MANE Select | ENSP00000264834.3:n.-44_-43insT | |
| NM_006563.3:c.-44_-43insT | NP_006554.1:n.-44_-43insT | |
| NM_006563.4:c.-44_-43insT | NP_006554.1:n.-44_-43insT | |
| NM_006563.5:c.-44_-43insT MANE Select | NP_006554.1:n.-44_-43insT |