Linked Data
gnomAD v4:
15-74751878-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74751879dup , CM000677.2:g.74751879dup | GRCh38 |
| NC_000015.9:g.75044220dup , CM000677.1:g.75044220dup | GRCh37 |
| NC_000015.8:g.72831273dup | NCBI36 |
| NG_008431.1:g.34338dup | |
| NG_008431.2:g.34338dup | |
| NG_061543.1:g.8035dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.1042+25dup MANE Select | ENSP00000342007.4:n.1042+25dup | |
| ENST00000343932.4:c.1042+25dup | ENSP00000342007.4:n.1042+25dup | |
| NM_000761.4:c.1042+25dup | NP_000752.2:n.1042+25dup | |
| NM_000761.5:c.1042+25dup MANE Select | NP_000752.2:n.1042+25dup |