Linked Data
dbSNP Id:
rs2134064901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672255_119672256del , CM000672.2:g.119672255_119672256del | GRCh38 |
| NC_000010.10:g.121431767_121431768del , CM000672.1:g.121431767_121431768del | GRCh37 |
| NC_000010.9:g.121421757_121421758del | NCBI36 |
| NG_016125.1:g.25886_25887del , LRG_742:g.25886_25887del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.508_509del | ||
| ENST00000369085.7:c.508_509del | ||
| ENST00000450186.1:c.334_335del | ||
| NM_004281.3:c.508_509del , LRG_742t1:c.508_509del | ||
| XM_005270287.1:c.508_509del | ||
| XM_005270287.2:c.508_509del | ||
| NM_004281.4:c.508_509del |