Linked Data
dbSNP Id:
rs774406294
gnomAD v2:
12-12871285-GC-G
gnomAD v3:
12-12718351-GC-G
gnomAD v4:
12-12718351-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.12718355del , CM000674.2:g.12718355del | GRCh38 |
| NC_000012.11:g.12871289del , CM000674.1:g.12871289del | GRCh37 |
| NC_000012.10:g.12762556del | NCBI36 |
| NG_016341.1:g.5988del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614874.2:c.475+41del | ENSP00000507272.1:n.475+41del | |
| ENST00000682620.1:n.1631-470del | ||
| ENST00000684771.1:n.585-470del | ||
| ENST00000228872.9:c.475+41del MANE Select | ENSP00000228872.4:n.475+41del | |
| ENST00000228872.8:c.475+41del | ENSP00000228872.4:n.475+41del | |
| ENST00000396340.1:c.475+41del | ENSP00000379629.1:n.475+41del | |
| ENST00000442489.1:c.193+302del | ENSP00000407597.1:n.193+302del | |
| ENST00000477087.1:n.155-470del | ||
| NM_004064.4:c.475+41del | NP_004055.1:n.475+41del | |
| NM_004064.5:c.475+41del MANE Select | NP_004055.1:n.475+41del |