Linked Data
gnomAD v4:
9-101421400-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101421406dup , CM000671.2:g.101421406dup | GRCh38 |
| NC_000009.11:g.104183688dup , CM000671.1:g.104183688dup | GRCh37 |
| NC_000009.10:g.103223509dup | NCBI36 |
| NG_012387.1:g.19380dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.*408dup MANE Select | ENSP00000497767.1:n.*408dup | |
| ENST00000374855.8:c.*408dup | ENSP00000363988.4:n.*408dup | |
| NM_000035.3:c.*408dup | NP_000026.2:n.*408dup | |
| NM_000035.4:c.*408dup MANE Select | NP_000026.2:n.*408dup |