Linked Data
dbSNP Id:
rs1960074260
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23211234_23211235del , CM000678.2:g.23211234_23211235del | GRCh38 |
| NC_000016.9:g.23222555_23222556del , CM000678.1:g.23222555_23222556del | GRCh37 |
| NC_000016.8:g.23130056_23130057del | NCBI36 |
| NG_011909.1:g.33516_33517del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300061.3:c.1177-800_1177-799del MANE Select | ENSP00000300061.2:n.1177-800_1177-799del | |
| ENST00000300061.2:c.1177-800_1177-799del | ENSP00000300061.2:n.1177-800_1177-799del | |
| NM_001039.3:c.1177-800_1177-799del | NP_001030.2:n.1177-800_1177-799del | |
| NM_001039.4:c.1177-800_1177-799del MANE Select | NP_001030.2:n.1177-800_1177-799del |