Linked Data
gnomAD v4:
15-74748914-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74748916dup , CM000677.2:g.74748916dup | GRCh38 |
| NC_000015.9:g.75041257dup , CM000677.1:g.75041257dup | GRCh37 |
| NC_000015.8:g.72828310dup | NCBI36 |
| NG_008431.1:g.31375dup | |
| NG_008431.2:g.31375dup | |
| NG_061543.1:g.5072dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.-10+19dup MANE Select | ENSP00000342007.4:n.-10+19dup | |
| ENST00000343932.4:c.-10+19dup | ENSP00000342007.4:n.-10+19dup | |
| NM_000761.4:c.-10+19dup | NP_000752.2:n.-10+19dup | |
| NM_000761.5:c.-10+19dup MANE Select | NP_000752.2:n.-10+19dup |