Linked Data
dbSNP Id:
rs1568505015
gnomAD v2:
19-36398498-CA-C
gnomAD v4:
19-35907596-CA-C
MyVariant Identifiers:
chr19:g.36398499del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35907597del , CM000681.2:g.35907597del | GRCh38 |
| NC_000019.9:g.36398499del , CM000681.1:g.36398499del | GRCh37 |
| NC_000019.8:g.41090339del | NCBI36 |
| NG_009304.1:g.5688del , LRG_607:g.5688del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262629.9:c.95-17del MANE Select | ENSP00000262629.3:n.95-17del | |
| ENST00000262629.8:c.95-17del | ENSP00000262629.3:n.95-17del | |
| ENST00000424586.7:c.62-17del | ENSP00000402371.3:n.62-17del | |
| ENST00000544690.6:c.62-17del | ENSP00000445332.1:n.62-17del | |
| ENST00000585626.1:n.162-17del | ||
| ENST00000585901.6:c.95-17del | ENSP00000468608.1:n.95-17del | |
| ENST00000586946.1:c.88-17del | ENSP00000465656.1:n.88-17del | |
| ENST00000587837.5:c.88-17del | ENSP00000465081.1:n.88-17del | |
| ENST00000588439.1:n.222del | ||
| ENST00000589517.1:c.95-17del | ENSP00000468447.1:n.95-17del | |
| NM_001173514.1:c.62-17del | NP_001166985.1:n.62-17del | |
| NM_001173515.1:c.62-17del | NP_001166986.1:n.62-17del | |
| NM_003332.3:c.95-17del , LRG_607t1:c.95-17del | NP_003323.1:n.95-17del | |
| NM_198125.2:c.95-17del | NP_937758.1:n.95-17del | |
| NR_033390.1:n.136-17del | ||
| NM_001173514.2:c.62-17del | NP_001166985.1:n.62-17del | |
| NM_001173515.2:c.62-17del | NP_001166986.1:n.62-17del | |
| NM_003332.4:c.95-17del MANE Select | NP_003323.1:n.95-17del | |
| NM_198125.3:c.95-17del | NP_937758.1:n.95-17del | |
| NR_033390.2:n.122-17del |