Linked Data
dbSNP Id:
rs759005688
ExAC:
1:152280191 GC / G
gnomAD v2:
1-152280191-GC-G
gnomAD v3:
1-152307715-GC-G
gnomAD v4:
1-152307715-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152307718del , CM000663.2:g.152307718del | GRCh38 |
| NC_000001.10:g.152280194del , CM000663.1:g.152280194del | GRCh37 |
| NC_000001.9:g.150546818del | NCBI36 |
| NG_016190.1:g.22488del , LRG_1028:g.22488del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.7170del MANE Select | ENSP00000357789.1:p.His2392IlefsTer27 | |
| ENST00000368799.1:c.7170del | ENSP00000357789.1:p.His2392IlefsTer27 | |
| NM_002016.1:c.7170del , LRG_1028t1:c.7170del | NP_002007.1:p.His2392IlefsTer27 | |
| XM_011509329.1:c.7170del | XP_011507631.1:p.His2392IlefsTer27 | |
| NM_002016.2:c.7170del MANE Select | NP_002007.1:p.His2392IlefsTer27 |