Linked Data
dbSNP Id:
rs1812199316
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837095del , CM000670.2:g.117837095del | GRCh38 |
| NC_000008.10:g.118849334del , CM000670.1:g.118849334del | GRCh37 |
| NC_000008.9:g.118918515del | NCBI36 |
| NG_007455.2:g.279726del , LRG_493:g.279726del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.523+14del | ||
| ENST00000378204.7:c.1056+14del MANE Select | ENSP00000367446.3:n.1056+14del | |
| ENST00000436216.2:c.424+14del | ||
| ENST00000378204.6:c.1056+14del | ENSP00000367446.2:n.1056+14del | |
| ENST00000436216.1:c.424+14del | ||
| ENST00000437196.1:c.74-1543del | ENSP00000407299.1:n.74-1543del | |
| NM_000127.2:c.1056+14del , LRG_493t1:c.1056+14del | NP_000118.2:n.1056+14del | |
| NM_000127.3:c.1056+14del MANE Select | NP_000118.2:n.1056+14del |