Canonical Allele Identifier:
CA573373492
Gene:
Linked Data
dbSNP Id:
rs1422150175
gnomAD v2:
7-24323061-TC-T
gnomAD v3:
7-24283442-TC-T
gnomAD v4:
7-24283442-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283447del , CM000669.2:g.24283447del | GRCh38 |
| NC_000007.13:g.24323066del , CM000669.1:g.24323066del | GRCh37 |
| NC_000007.12:g.24289591del | NCBI36 |
| NG_016148.1:g.4260del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017012910.1:c.42-27744del | XP_016868399.1:n.42-27744del | |
| XM_017012911.1:c.42-27744del | XP_016868400.1:n.42-27744del | |
| XR_001745121.1:n.473+35914del | ||
| XR_001745122.1:n.345-86414del | ||
| XR_001745123.1:n.473+35914del | ||
| XR_001745124.1:n.473+35914del | ||
| XR_001745125.1:n.473+35914del | ||
| XR_001745126.1:n.473+35914del | ||
| XR_001745127.1:n.345-27744del | ||
| XR_001745129.1:n.473+35914del | ||
| XR_001745130.1:n.473+35914del | ||
| XR_001745131.1:n.473+35914del | ||
| XR_001745132.1:n.473+35914del |