Linked Data
gnomAD v4:
18-13884519-A-AG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.13884522dup , CM000680.2:g.13884522dup | GRCh38 |
| NC_000018.9:g.13884521dup , CM000680.1:g.13884521dup | GRCh37 |
| NC_000018.8:g.13874521dup | NCBI36 |
| NG_011819.1:g.36017dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327606.4:c.*105dup MANE Select | ENSP00000333821.2:n.*105dup | |
| ENST00000327606.3:c.*105dup | ENSP00000333821.2:n.*105dup | |
| NM_000529.2:c.*105dup MANE Select | NP_000520.1:n.*105dup | |
| NM_001291911.1:c.*105dup | NP_001278840.1:n.*105dup | |
| XM_017025781.1:c.*105dup | XP_016881270.1:n.*105dup |