Linked Data
dbSNP Id:
rs1741430905
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44359663del , CM000667.2:g.44359663del | GRCh38 |
| NC_000005.9:g.44359765del , CM000667.1:g.44359765del | GRCh37 |
| NC_000005.8:g.44395522del | NCBI36 |
| NG_011446.1:g.34021del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264664.5:c.325+28696del MANE Select | ENSP00000264664.4:n.325+28696del | |
| ENST00000264664.4:c.325+28696del | ENSP00000264664.4:n.325+28696del | |
| NM_004465.1:c.325+28696del | NP_004456.1:n.325+28696del | |
| XM_005248264.2:c.325+28696del | XP_005248321.1:n.325+28696del | |
| XM_005248264.4:c.325+28696del | XP_005248321.1:n.325+28696del | |
| NM_004465.2:c.325+28696del MANE Select | NP_004456.1:n.325+28696del |