Linked Data
gnomAD v4:
7-19117214-TCCC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117217_19117219del , CM000669.2:g.19117217_19117219del | GRCh38 |
| NC_000007.13:g.19156840_19156842del , CM000669.1:g.19156840_19156842del | GRCh37 |
| NC_000007.12:g.19123365_19123367del | NCBI36 |
| NG_008114.1:g.5456_5458del | |
| NG_008114.2:g.5456_5458del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.105_107del MANE Select | ENSP00000242261.5:p.Gly36del | |
| ENST00000242261.5:c.105_107del | ENSP00000242261.5:p.Gly36del | |
| NM_000474.3:c.105_107del | NP_000465.1:p.Gly36del | |
| XM_011515496.1:c.105_107del | XP_011513798.1:p.Gly36del | |
| NR_149001.1:n.456_458del | ||
| NM_000474.4:c.105_107del MANE Select | NP_000465.1:p.Gly36del | |
| NR_149001.2:n.420_422del |