Linked Data
gnomAD v4:
19-615966-CGCA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.615968_615970del , CM000681.2:g.615968_615970del | GRCh38 |
| NC_000019.9:g.615968_615970del , CM000681.1:g.615968_615970del | GRCh37 |
| NC_000019.8:g.566968_566970del | NCBI36 |
| NG_023049.1:g.22600_22602del | |
| NG_052810.1:g.31076_31078del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251287.3:c.2164_2166del MANE Select | ENSP00000251287.1:p.Gln722del | |
| ENST00000251287.2:c.2164_2166del | ENSP00000251287.1:p.Gln722del | |
| NM_001194.3:c.2164_2166del | NP_001185.3:p.Gln722del | |
| NM_001194.4:c.2164_2166del MANE Select | NP_001185.3:p.Gln722del |