Linked Data
dbSNP Id:
rs1867444499
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585139del , CM000673.2:g.67585139del | GRCh38 |
| NC_000011.9:g.67352610del , CM000673.1:g.67352610del | GRCh37 |
| NC_000011.8:g.67109186del | NCBI36 |
| NG_012075.1:g.6545del , LRG_723:g.6545del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398603.6:c.234del | ||
| ENST00000398606.10:c.234del | ||
| ENST00000646888.1:c.127del | ||
| ENST00000398603.5:c.234del | ||
| ENST00000398606.7:c.234del | ||
| ENST00000467591.1:n.345del | ||
| ENST00000494593.1:n.1029del | ||
| ENST00000498765.5:c.297del | ||
| NM_000852.3:c.234del , LRG_723t1:c.234del | ||
| NM_000852.4:c.234del |